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Pharmacotherapy for trichotillomania

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Background

Trichotillomania (TTM; hair‐pulling disorder) is a prevalent and disabling disorder characterised by recurrent hair‐pulling. Here we update a previous Cochrane Review on the effects of medication for TTM.

Objectives

To assess the effects of medication for trichotillomania (TTM) in adults, children and adolescents compared with placebo or other medication.

Search methods

We searched CENTRAL, MEDLINE, Embase, PsycINFO, eleven other bibliographic databases, trial registries and grey literature sources (to 26 November 2020). We checked reference lists and contacted subject experts.

Selection criteria

We selected randomised controlled trials of medication versus placebo or other medication for TTM in adults, children and adolescents.

Data collection and analysis

We used standard methodological procedures expected by Cochrane.

Main results

Twelve studies were included. We identified 10 studies in adults (286 participants) with a mean sample size of 29 participants per trial; one study in children and adolescents (39 participants); and, one study in adults and adolescents (22 participants: 18 adults and 4 adolescents). All studies were single‐centre, outpatient trials. Eleven studies compared medication and placebo (334 participants); one study compared two medications (13 participants). Studies were 5 to 13 weeks duration. We undertook meta‐analysis only for opioid antagonists as other comparisons contained a single study, or reported insufficient data.

Antioxidants versus placebo in adults

There was little to no difference in treatment response between antioxidant (35.7%) and placebo groups (28.6%) after six weeks, based on a single trial of silymarin (risk ratio (RR) 2.25, 95% confidence interval (CI) 0.84 to 5.99; 36 participants; low‐certainty evidence). We could not calculate differences in number of dropouts as there were no events in either group (18 participants; low‐certainty evidence).

Antioxidants versus placebo in adolescents

There was little to no difference in treatment response between antioxidant (50%) and placebo groups (25%) after six weeks, based on a single trial of silymarin (RR 2.00, 95% CI 0.28 to 14.20; 8 participants; low‐certainty evidence). We could not calculate differences in number of dropouts as there were no events in either group (8 participants; low‐certainty evidence).

Antipsychotics versus placebo in adults

There may be greater treatment response in the antipsychotic group (85%) compared to the placebo group (17%) after 12 weeks, based on a single trial of olanzapine (RR 5.08, 95% CI 1.4 to 18.37; 25 participants; low‐certainty evidence). We could not calculate differences in number of dropouts as there were no events in either group (25 participants; low‐certainty evidence).

Cell signal transducers versus placebo in adults

There was little to no difference in treatment response between cell signal transducer (42.1%) and placebo groups (31.6%) after 10 weeks, based on a single trial of inositol (RR 1.33, 95% CI 0.57 to 3.11; 38 participants; low‐certainty evidence). We could not calculate differences in number of dropouts as there were no events in either group (38 participants; low‐certainty evidence).

Glutamate modulators versus placebo in adults

There is probably greater treatment response in the glutamate modulator group (56%) compared to the placebo group (16%) after 12 weeks, based on a single trial of N‐acetylcysteine (RR 3.5, 95% CI 1.34 to 9.17; 50 participants; moderate‐certainty evidence). We could not calculate differences in number of dropouts as there were no events in either group (50 participants; low‐certainty evidence).

Glutamate modulators versus placebo in children and adolescents

There was little to no difference in treatment response between the glutamate modulator (25%) and placebo groups (21.1%) in children and adolescents, based on a single trial of N‐acetylcysteine (RR 1.19, 95% CI 0.37 to 3.77; 39 participants; low‐certainty evidence). There was little to no difference in dropouts due to adverse events between glutamate modulator (5%) and placebo (0%) groups, based on a single trial (RR 2.86, 95% CI 0.12 to 66.11; 39 participants; low‐certainty evidence).

Opioid antagonists versus placebo in adults

There may be little to no difference in treatment response between opioid antagonist (37.5%) and placebo groups (25%) after six to eight weeks, based on two studies of naltrexone, but the evidence is very uncertain (RR 2.14, 95% CI 0.25 to 18.17; 2 studies, 68 participants; very low‐certainty evidence). No data were available regarding dropouts due to adverse events.

Selective serotonin reuptake inhibitors (SSRIs) versus placebo in adults

There were no data available for treatment response to SSRIs. There was little to no difference in dropouts due to adverse events in the SSRI group (5.1%) compared to the placebo group (0%) after 6 to 12 weeks, based on two trials of fluoxetine (RR 3.00, 95% CI 0.33 to 27.62; 2 studies, 78 participants; low‐certainty evidence).

Tricyclic antidepressants (TCAs) with predominantly serotonin reuptake inhibitor (SRI) actions versus placebo in adults

There may be greater treatment response in the TCAs with predominantly SRI actions group (40%) compared to the placebo group (0%) after nine weeks, but the evidence is very uncertain, based on a single trial of clomipramine (RR 5.73, 95% CI 0.36 to 90.83; 16 participants; very low‐certainty evidence). There may be increased dropouts due to adverse events in the TCAs with predominantly SRI actions group (30%) compared to the placebo group (0%), but the evidence is very uncertain (RR 4.45, 95% CI 0.27 to 73.81; 16 participants; very low‐certainty evidence).

TCAs with predominantly SRI actions versus other TCAs in adults

There may be greater treatment response in the TCAs with predominantly SRI actions group compared to the other TCAs group after five weeks, based on a single trial comparing clomipramine to desipramine (mean difference (MD) ‐4.00, 95% CI ‐6.13 to ‐1.87; 26 participants; low‐certainty evidence). We could not calculate differences in number of dropouts as there were no events in either group (26 participants; low‐certainty evidence).

Authors' conclusions

There was insufficient evidence from meta‐analysis to confirm or refute the efficacy of any agent or class of medication for the treatment of TTM in adults, children or adolescents. Preliminary evidence suggests there may be beneficial treatment effects for N‐acetylcysteine, clomipramine and olanzapine in adults based on four trials, albeit with relatively small sample sizes.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Drug treatments for chronic hair‐pulling (trichotillomania)

Trichotillomania (TTM) is a common and disabling condition characterised by repeated hair‐pulling leading to hair loss. TTM can be associated with much distress and impairment. It may also be associated with other psychiatric conditions (known as comorbidities) such as depression and anxiety disorders. Researchers have proposed that medication may be useful to treat this condition.

Who will be interested in this review?

‐ People with TTM or other common comorbidities.

‐ Families and friends of people who have TTM or other common comorbidities.

‐ Mental health clinicians, general practitioners, psychiatrists, psychologists and pharmacists.

What questions does this review aim to answer?

‐ Is medication an effective treatment for TTM in adults or children and adolescents? That is, does it have the intended result?

‐ Does medication reduce the severity of symptoms for adults or children and adolescents with TTM?

‐ Does medication aid in treating symptoms of depression in adults or children and adolescents with TTM?

‐ Is medication effective and tolerable for people with TTM in terms of side effects?

‐ Does medication improve quality of life and reduce disability?

Which studies were included in the review?

‐ We included nine studies comparing a medication with a placebo (control substance/not an active drug) for the treatment of TTM in adults.

‐ We included one study comparing two different antidepressant drugs with each other for the treatment of TTM in adults.

‐ We included one study comparing a medication with a placebo for the treatment of TTM in children and adolescents aged 8 to 17 years.

‐ We included one study comparing a medication with a placebo for the treatment of TTM in adolescents and adults aged 12 to 65 years.

‐ A total of 298 adults were included from the 11 studies conducted in adults, and a total of 43 children and adolescents were included from the two trials conducted with participants in this age group.

What does the evidence from the review tell us?

There was insufficient evidence from analysis of individual studies or across multiple scientific studies (known as meta‐analysis) to confirm or refute the effectiveness of any specific agent or class of medication for the treatment of TTM in adults, children or adolescents. In adults, evidence suggests tricyclic antidepressants (TCAs; a type of antidepressant) with predominantly serotonin reuptake inhibitor (SRI; increasing serotonin levels in the brain) actions may show a beneficial treatment effect compared to other TCAs, with reduction in TTM symptom severity. However, certainty in the estimate of effect was low and is based on a single trial comparing clomipramine with desipramine. Antipsychotics in adults may show a beneficial treatment effect and possible reduction of TTM symptom severity, with low‐certainty in the estimate of effect, based on a single trial of olanzapine. Glutamate modulators (a type of amino acid modulator) in adults showed a probable beneficial treatment effect and a likely reduction in TTM symptom severity, with moderate‐certainty in the estimate of effect, although based on a single trial of N‐acetylcysteine (NAC; a glutamate modulator). Glutamate modulators in children and adolescents (8 to 17 years old) showed no evidence for beneficial effect in terms of the percentage of participants responding to treatment in a single study of NAC. However, evidence suggests a potential large reduction in TTM symptom severity; however, with low‐certainty in the estimate. There was little to no evidence for beneficial treatment effects in terms of the percentage of participants responding to treatment or reduction of TTM symptom severity reported for antioxidants, cell signal transducers, opioid antagonists or selective serotonin reuptake inhibitors (SSRIs; a type of antidepressant) in adults, children or adolescents.

Attrition due to adverse events was only reported for SSRIs and TCAs with predominantly SRI actions in adults and for glutamate modulators in children and adolescents. Glutamate modulators had the least severe side effect profile in adults, while antipsychotics were associated with several adverse side effects, although with low‐certainty in the effect estimate, and based on individual trials for each medication class. There was low‐certainty evidence showing no difference in dropouts due to adverse events between the glutamate modulator group and placebo group in the single study exclusively in children and adolescents.

What should happen next?

There is some evidence that NAC (a glutamate modulator) probably demonstrates efficacy in TTM in adults and possible symptom severity reduction in children and adolescents. There is some evidence that olanzapine (an antipsychotic) and clomipramine (a TCA with predominantly SRI actions) may demonstrate efficacy in TTM in adults, although based on individual trials and therefore not generalisable to other agents in the same medication classes. Studies are few and sample sizes are small, and as a result it is not possible to draw high‐quality conclusions from meta‐analysis. Additional studies, with rigorous designs and appropriately powered samples are needed, particularly in children and adolescents. Future studies could also include people with common comorbidities, as the current evidence base may not be representative of clinical populations, who might have multiple medical and psychiatric conditions.

Authors' conclusions

Implications for practice

There was insufficient evidence from meta‐analysis to confirm or refute efficacy of any particular agent or class of medication in the treatment of trichotillomania (TTM) for any age group. Preliminary evidence has suggested beneficial treatment effects of tricyclic antidepressants (TCAs) with predominantly serotonin reuptake inhibitor (SRI) actions (clomipramine 50 mg titrated up to 250 mg per day; low‐certainty evidence), glutamate modulators (N‐acetylcysteine (NAC) 1200 mg per day titrated up to 1200 mg twice daily; moderate‐certainty evidence) and antipsychotics (olanzapine 2.5 mg per day titrated up to 10 mg per day; low‐certainty evidence) in adults, based on three individual trials, all of which had relatively small sample sizes (Grant 2009; Swedo 1989; Van Ameringen 2010). There is some low‐certainty evidence that NAC reduces TTM symptom severity in children, also based on a single trial (Bloch 2013).

Implications for research

The existing evidence base of randomised controlled trials includes a mixture of parallel and cross‐over trials, participants with a range of comorbid disorders and the use of unpublished rating scales. In addition, the existing trials have relatively small sample sizes, and the body of evidence is of low‐certainty because of high attrition rates and lack of intention‐to‐treat analyses. In the future, trials on a variety of agents, of longer duration, with larger sample sizes and using validated rating instruments (such as the Clinical Global Impressions‐Improvement (CGI‐I) and the Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)) are needed. Additionally, inclusion of participants with common comorbidities is encouraged, to better reflect clinical populations. Given the preliminary evidence presented in four small trials of a glutamate modulator, an antipsychotic and a TCA with predominantly SRI actions, further work on these three classes of drugs is needed (Bloch 2013; Grant 2009; Swedo 1989; Van Ameringen 2010). Studies of other classes, such as SNRIs, may be useful in determining differential effects of serotonergic and noradrenergic agents in the treatment of TTM. Whilst preliminary evidence is encouraging, more studies in children and adolescents are required to investigate the effects of NAC seen in these age groups, and to investigate the efficacy of other agents in children.

Summary of findings

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Summary of findings 1. Antioxidants versus placebo for trichotillomania in adults

Antioxidants versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: antioxidants versus placebo in adults

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Antioxidants versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) or similar (no. of responders)

Follow‐up: 6 weeks

Study population

RR 2.25
(0.84 to 5.99)

36
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the antioxidant group and the placebo group in adults.

222 per 1000

500 per 1000
(187 to 1000)

Moderate

222 per 1000

500 per 1000
(186 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 6 weeks

The mean MGH‐HPS score for the antipsychotic intervention group was 12.5.

The mean reduction of TTM symptom severity in the intervention groups was 1.8 lower
(6.22 lower to 2.62 higher).

27
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the antioxidant group compared to the placebo group on the MGH‐HPS in adults.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate

Follow‐up: 6 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

18
(1 study)

⊕⊕⊝⊝
lowb

The evidence is uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).

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Summary of findings 2. Antioxidants versus placebo for trichotillomania in adolescents

Antioxidants versus placebo for trichotillomania in adolescents

Patient or population: children with trichotillomania
Settings: outpatient
Intervention: antioxidants versus placebo in adolescents

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Antioxidants versus placebo in adolescents

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) or similar (no. of responders)

Follow‐up: 6 weeks

Study population

RR 2
(0.28 to 14.2)

8
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the antioxidant group and the placebo group in adolescents.

250 per 1000

500 per 1000
(70 to 1000)

Moderate

333 per 1000

666 per 1000
(110 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 6 weeks

The mean MGH‐HPS score for the antipsychotic intervention group was 6.83.

The mean reduction of TTM symptom severity in the intervention groups was
5.87 lower
(17.46 lower to 5.72 higher).

6
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the antioxidant group compared to the placebo group on the MGH‐HPS in adolescents.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate

Follow‐up: 6 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

6
(1 study)

⊕⊕⊝⊝
lowb

The evidence is uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).

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Summary of findings 3. Antipsychotics versus placebo for trichotillomania in adults

Antipsychotics versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: antipsychotics

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Antipsychotics versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I)

(no. of responders)

Follow‐up: 12 weeks

Study population

RR 5.08
(1.4 to 18.37)

25
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence of benefit on the number of participants who responded to treatment in the antipsychotic group compared to the placebo group.

167 per 1000

847 per 1000
(233 to 1000)

Moderate

167 per 1000

848 per 1000
(234 to 1000)

Reduction of TTM symptom severity
Massachusetts General

Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 12 weeks

The mean MGH‐HPS score for the antipsychotic intervention group was 8.38.

The mean reduction of TTM symptom severity in the intervention group was
4.87 points lower
(8.84 to 0.9 lower).

25
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence for a reduction of TTM symptom severity in the antipsychotic group compared to the placebo group on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate
Follow‐up: 12 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

25
(1 study)

⊕⊕⊝⊝
lowc

The evidence was uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to very small sample size ( < 50).
cDowngraded by two levels due to zero events and very small sample size ( < 50).

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Summary of findings 4. Cell signal transducers versus placebo for trichotillomania in adults

Cell signal transducers versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: cell signal transducers

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Cell signal transducers versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

Follow‐up: 10 weeks

Study population

RR 1.33
(0.57 to 3.11)

38
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the cell signal transducer group and the placebo group.

316 per 1000

420 per 1000
(180 to 982)

Moderate

316 per 1000

420 per 1000
(180 to 983)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 10 weeks

The mean MGH‐HPS score for the cell signal transducer intervention group was 13.2.

The mean reduction of TTM symptom severity in the intervention groups was
1.3 points lower
(5.12 lower to 2.52 higher).

38
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the cell signal transducer group compared to the placebo group on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate
Follow‐up: 10 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

38
(1 study)

⊕⊕⊝⊝
lowc

The evidence was uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
cDowngraded by two levels due to zero events and very small sample size ( < 50).

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Summary of findings 5. Glutamate modulators versus placebo for trichotillomania in adults

Glutamate modulators versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: glutamate modulators

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Glutamate modulators versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

Follow‐up: 12 weeks

Study population

RR 3.5
(1.34 to 9.17)

50
(1 study)

⊕⊕⊕⊝
moderateb

There was moderate‐certainty evidence of benefit on the number of participants who responded to treatment in the glutamate modulator group compared to the placebo group in adults.

160 per 1000

560 per 1000
(214 to 1000)

Moderate

160 per 1000

560 per 1000
(214 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 12 weeks

The mean MGH‐HPS score for the glutamate modulator intervention group was 10.4.

The mean reduction of TTM symptom severity in the intervention groups was
5.6 points lower
(8.5 to 2.7 lower).

50
(1 study)

⊕⊕⊕⊝
moderateb

There was moderate‐certainty evidence for a reduction of TTM symptom severity in the glutamate modulator group compared to the placebo group on the MGH‐HPS in adults.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate
Follow‐up: 12 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

50
(1 study)

⊕⊕⊝⊝
lowc

The evidence was uncertain about the effect of dropouts due to adverse events in adults.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to small sample size (50 to 400).
cDowngraded by two levels due to zero events and small sample size (50 to 400).

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Summary of findings 6. Glutamate modulators versus placebo for trichotillomania in children and adolescents

Glutamate modulators versus placebo for trichotillomania in children and adolescents

Patient or population: children and adolescents with trichotillomania
Settings: outpatient
Intervention: glutamate modulators

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Glutamate modulators versus placebo in children and adolescents

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

Follow‐up: 12 weeks

Study population

RR 1.19
(0.37 to 3.77)

39
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the glutamate modulator group and the placebo group in children and adolescents.

211 per 1000

251 per 1000
(78 to 794)

Moderate

211 per 1000

251 per 1000
(78 to 795)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 12 weeks

The mean MGH‐HPS score for the glutamate modulator intervention group was 10.7.

The mean reduction of TTM symptom severity in the intervention groups was
2.83 points lower
(3.76 to 1.9 lower).

39
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence for a potentially large reduction of TTM symptom severity in the glutamate modulator group compared to the placebo group on the MGH‐HPS in children and adolescents.

Tolerability of treatment ‐ dropouts due to adverse eventsc
Dropout rate

Follow‐up: 12 weeks

Study population

RR 2.86
(0.12 to 66.11)

39
(1 study)

⊕⊕⊝⊝
lowd

There was low‐certainty evidence showing no difference in dropouts due to adverse events between groups.

N = 0/19

N = 1/20

Moderate

N = 0/19

N = 1/20

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to very small sample size ( < 50).
cNumbers presented as raw values for N (events) in study population (intervention and control groups), and not modelled on RR.
dDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).

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Summary of findings 7. Opioid antagonists versus placebo for trichotillomania in adults

Opioid antagonists versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: opioid antagonists

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Opioid antagonists versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders) & NIMH Trichotillomania Severity Scale (NIMH‐TSS)

(no. of responders as > 50% reduction)

Follow‐up: 6 to 8 weeks

Study population

RR 2.14
(0.25 to 18.17)

68
(2 studies)

⊕⊝⊝⊝
very lowb,c

There is very uncertain evidence showing no effect of opioid antagonists on treatment response.

250 per 1000

535 per 1000
(62 to 1000)

Moderate

173 per 1000

370 per 1000
(43 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 8 weeks

The mean MGH‐HPS score for the opioid antagonist intervention group was 12.21.

The mean reduction of TTM symptom severity in the intervention groups was
1.14 points lower
(4.18 lower to 1.9 higher).

51
(1 study)

⊕⊕⊝⊝
lowc

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the opioid antagonist group compared to the placebo group on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse events

See comment

See comment

No data available for this outcome.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to moderate heterogeneity (I² = 59%)
cDowngraded by two levels due to wide confidence interval and small sample size (50 to 400).

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Summary of findings 8. SSRIs versus placebo for trichotillomania in adults

SSRIs versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: SSRIs

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

SSRIs versus placebo in adults

Treatment response

See comment

See comment

No data available for this outcome.

Reduction of TTM symptom severitya
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS) mean change score

Follow‐up: 12 weeks

The mean change of the MGH‐HPS score for the SSRI intervention group was ‐1.5333.

The mean reduction of TTM symptom severity in the intervention groups was
0.47 points lower
(4.3 lower to 3.36 higher).

31
(1 study)

⊕⊝⊝⊝
very lowb,c,d

The evidence is very uncertain about the effect of SSRIs on reduction of TTM symptom severity on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse eventse
Dropout rate

Follow‐up: 6 to 12 weeks

Study population

RR 3
(0.33 to 27.62)

78
(2 studies)

⊕⊕⊝⊝
lowf

There was low‐certainty evidence showing no difference in dropouts due to adverse events between groups.

N = 0/39

N = 2/39

Moderate

N = 0/39

N = 2/39

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to serious risk of bias. Concerns with attrition bias. Intention‐to‐treat analysis not used. No reasons for attrition given.
cDowngraded by one level as mean and standard deviations at endpoint were unavailable. Data provided from correspondence were mean change scores from baseline to endpoint.
dDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
eNumbers presented as raw values for N (events) in study population (intervention and control groups), and not modelled on RR.
fDowngraded by two levels due to wide confidence interval and small sample size (50 to 400).

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Summary of findings 9. TCAs with predominantly SRI actions versus placebo for trichotillomania in adults

TCAs with predominantly SRI actions versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: TCAs with predominantly SRI actions

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

TCAs with predominantly SRI actions versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CG‐I) (no. of responders)

Follow‐up: 9 weeks

Study population

RR 5.73
(0.36 to 90.83)

16
(1 study)

⊕⊝⊝⊝
very lowb,c

The evidence is very uncertain about the effect of TCAs with predominantly SRI actions on treatment response.

0 per 1000

0 per 1000
(0 to 0)

Moderate

0 per 1000

0 per 1000
(0 to 0)

Reduction of TTM symptom severity
NIMH Trichotillomania Severity Scale (NIMH‐TSS)

Follow‐up: 9 weeks

The mean NIMH‐TSS score for the TCA with predominantly SRI actions intervention group was 9.3.

The mean reduction of TTM symptom severity in the intervention group was
3 points lower
(6.52 lower to 0.52 higher).

16
(1 study)

⊕⊝⊝⊝
very lowb,c

The evidence is very uncertain about the effect of TCAs with predominantly SRI actions on reduction of TTM symptom severity on the NIMH‐TSS.

Tolerability of treatment ‐ dropouts due to adverse eventsd
Dropout rate

Follow‐up: 9 weeks

Study population

RR 4.45
(0.27 to 73.81)

16
(1 study)

⊕⊝⊝⊝
very lowb,c

The evidence is very uncertain about the effect of TCAs with predominantly SRI actions on dropouts due to adverse events.

N = 0/6

N = 3/10

Moderate

N = 0/6

N = 3/10

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to serious risk of bias. Concerns with attrition bias. Intention‐to‐treat analysis not used, 3 withdrew from clomipramine group due to adverse events. 40% overall attrition rate in clomipramine group.
cDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
dNumbers presented as raw values for N (events) in study population (intervention and control groups), and not modelled on RR.

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Summary of findings 10. TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults

TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: TCAs with predominantly SRI actions

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

TCAs with predominantly SRI actions versus other TCAs in adults

Treatment responsea
Physician‐rated Clinical

Progress Scale

Follow‐up: 5 weeks

The mean Physician‐rated Clinical Progress Scale score for the TCA with predominantly SRI actions intervention group was 4.7.

The mean treatment response in the intervention group was
4 points lower
(6.13 to 1.87 lower).

26
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence for a beneficial effect on treatment response in the TCAs with predominantly SRI actions group compared to the other TCAs group on the Physician‐rated Clinical Progress Scale.

Reduction of TTM symptom severity
NIMH Trichotillomania Severity Scale (NIMH‐TSS)

Follow‐up: 5 weeks

The mean NIMH‐TSS score for the TCA with predominantly SRI actions intervention group was 10.6

The mean reduction of TTM symptom severity in the intervention groups was
3.8 points lower
(8.08 lower to 0.48 higher).

26
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence of no difference in reduction of TTM symptom severity in the TCAs with predominantly SRI actions group compared to the other TCAs group on the NIMH‐TSS.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate

Follow‐up: 5 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

26
(1 study)

⊕⊕⊝⊝
lowc

The evidence is uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
cDowngraded by two levels due to zero events and very small sample size ( < 50).

Background

Description of the condition

Trichotillomania (TTM) is a disorder characterised by recurrent hair‐pulling, resulting in hair loss (APA 2012). It was first named in 1889 by François Henri Hallopeau, a French dermatologist (França 2019). The introduction of TTM into the Diagnostic and Statistical Manual of Mental Disorders, Third Edition, Revised (DSM‐III‐R) encouraged treatment studies to proceed. In the DSM‐III‐R, TTM was conceptualised as an impulse‐control disorder not elsewhere classified. TTM, kleptomania, pyromania and other conditions in the category were characterised by failure to resist an impulse, drive or temptation to perform an act that is harmful to the self or others (APA 1987). TTM remained under Impulse‐Control Disorders in DSM‐IV.

Based on the diagnostic criteria presented in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM‐5) (APA 2012), a diagnosis of TTM requires that recurrent hair‐pulling must result in hair loss (criterion A). Evidence of an attempt to decrease or stop hair‐pulling must also be present (criterion B). Furthermore, the diagnosis of TTM can be made only if hair‐pulling is not better accounted for by another disorder (e.g. in response to a delusion, or as part of a body dysmorphic disorder) and is not a result of a general medical condition (criterion C). Finally, for a diagnosis of TTM, recurrent hair‐pulling must cause significant distress or impairment of functioning (criterion D).

The Trichotillomania Impact Project has emphasised the immense distress and impairment associated with chronic hair‐pulling (Woods 2006). People with TTM often have low levels of self‐esteem, low psychosocial functioning and other comorbid psychiatric disorders, especially mood and anxiety disorders (Grant 2016; Lochner 2019; Stein 2010). Other body‐focused repetitive behaviours (BFRBs) are also important comorbidities that may worsen the severity of the primary disorder (Grant 2016). Community prevalence studies indicate that TTM is a common disorder with a point prevalence estimate of 0.5% to 2.0% (Grant 2016). In recent years, the prevalence of TTM and other BFRBs has been estimated as significantly higher. In a survey of 82 college students, Odlaug 2010 found a prevalence rate of 3.91% for TTM, and in a large study of 4335 college students, Houghton 2018 found that 12.27% of students met criteria for a clinically significant BFRB, including TTM. The onset of TTM is often in childhood (Odlaug 2012); thus, it is important to have effective treatments that have been tested in the young age group.

Some overlap has been noted between TTM and conditions such as obsessive‐compulsive disorder (OCD) (Grant 2007). Many people report that hair‐pulling is preceded by urges, and that hair‐pulling involves ritualistic behaviours redolent of OCD (Swedo 1992). Early work suggested that people with TTM and people with OCD respond to selective serotonin reuptake inhibitors (SSRIs) (Swedo 1989). This and related research led to the inclusion of TTM in a new section of DSM‐5, entitled 'Obsessive‐Compulsive and Related Disorders' (OCRD) (APA 2012), as well as under OCRDs in the BFRB subcategory in the International Classification of Diseases ‐ 11th revision (ICD‐11) (WHO 2018).

Whilst TTM is currently categorised as an OCRD, there are also important differences between TTM and OCD in symptomatology, as well as in treatment response. TTM is not characterised by obsessive thoughts, and greater overlap may be evident with other obsessive‐compulsive spectrum disorders, such as skin‐picking and tic disorders (Stein 2010). Findings that TTM responds to low‐dose antipsychotics and not to SSRIs are redolent of findings on the pharmacotherapy of tic disorders (Eddy 2011). Neuroimaging and treatment studies have strengthened the relationship between TTM and tic disorders (Lamothe 2019). The phenomenology and treatment of TTM may be closer to those of tic disorders than OCD; therefore, it may be helpful to consider TTM as a tic disorder in clinical practice (Lamothe 2019).

Research on the psychobiology of TTM has increased in recent decades; however, specific mechanisms are yet to be established. A review of the neurobiology of TTM shows that researchers have studied numerous regions of interest in relation to TTM across all cerebral lobes, involving white and grey matter, in cortical and subcortical structures. These include the basal ganglia, amygdala, hippocampus, cerebellum and somatosensory cortex (Chamberlain 2009). White matter tracts involved in habit generation and suppression have also been implicated (Grant 2016). In a functional neuroimaging study (N = 10) using single‐photon emission computed tomography (SPECT), 12 weeks of treatment with 20 mg of citalopram, titrated to a maximum dose of 60 mg, was associated with reduced activation in frontal and striatal regions (Stein 2002).

Several different pharmacotherapy and psychotherapy interventions have been studied in the treatment of TTM. Medications, cognitive‐behavioural therapy (CBT) and their combination have been studied in a number of randomised controlled trials (RCTs) and meta‐analyses (Bloch 2007; França 2019; Grant 2016; Jafferany 2018; McGuire 2014; Rehm 2015). Meta‐analysis of clomipramine and other serotonin reuptake inhibitors (SRIs) in TTM found a significant beneficial treatment effect (Bloch 2007; McGuire 2014). In a more recent meta‐analysis, selective serotonin reuptake inhibitors (SSRIs) were shown to have no benefit, whilst clomipramine demonstrated a benefit in reducing TTM symptoms (Farhat 2020). In terms of psychotherapy specifically, habit‐reversal therapy (HRT) may have efficacy in the treatment of TTM (Bloch 2007; França 2019; Grant 2016; McGuire 2014). These findings are limited by the small number of individual trials, a lack of trials targeted at children and adolescents, a lack of long‐term follow‐up to establish durability of treatment and a lack of acknowledgement of comorbidities (Lee 2019). Whilst pharmacotherapy and psychotherapy have both been utilised for the treatment of TTM, this review focuses on medication.

Description of the intervention

Early studies of treatment of TTM in adults focused on the use of antidepressants such as SSRIs (e.g. citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline; Christenson 1991a; Christenson 1998; Dougherty 2006; Gabriel 2001; Gadde 2007; Iancu 1996; Koran 1992; Mahr 1993; Stanley 1991; Stein 1997; Streichenwein 1995; Winchel 1992), serotonin‐noradrenaline reuptake inhibitors (SNRIs; e.g. venlafaxine; Ninan 1998), and tricyclic antidepressants (TCAs) with predominantly serotonin reuptake inhibitor (SRI) actions (e.g. clomipramine; Black 1992; Ninan 2000; Pollard 1991; Swedo 1989). Other traditional psychotropic agents have also been studied, including antipsychotic agents (e.g. haloperidol, olanzapine, quetiapine, risperidone; Epperson 1999; Sentürk 2002; Van Ameringen 1999; Van Ameringen 2010; White 2011; Yasui‐Furukori 2011), mood stabilisers (e.g. lithium; Sharma 2008), anticonvulsant agents (e.g. gabapentin, lamotrigine, levetiracetam, tiagabine, topiramate; Adewuya 2008; Leombruni 2010; Lochner 2006), opioid antagonists (e.g. naltrexone; De Sousa 2008; Grant 2014), and other antidepressants such as bupropion (Klipstein 2012). More recent studies have investigated a range of different agents from other classes such as cell signal transducers (e.g. inositol; Leppink 2017), cannabinoids (e.g. dronabinol; Grant 2011), and antioxidants (e.g. silymarin; Grant 2015; Grant 2019). In particular, the use of N‐acetylcysteine (NAC), a glutamate modulator, has been increasingly examined in recent years in adults and children, with varying results (Bloch 2013; França 2017; Grant 2009; Odlaug 2007; Rodrigues‐Barata 2012; Silva‐Netto 2014; Stewart 2003; Taylor 2014).

Few studies examine the effects of medication specifically in children and adolescents under 18 years old (Adewuya 2008; Bloch 2013; De Sousa 2008; Golubchik 2011). To date, NAC is the only drug studied under randomised, placebo‐controlled conditions in children and adolescents with TTM (Bloch 2013). Naltrexone has shown promising results in an open‐label pilot study in children with TTM (De Sousa 2008). Valproic acid has also shown good results, albeit in a single case study (Adewuya 2008).

How the intervention might work

Several functional pathways have been hypothesised to be involved in TTM, involving affect regulation, behavioural addiction and cognitive control (Stein 2006). Certain neuroanatomical structures, including areas of the basal ganglia, amygdala, hippocampus, cerebellum and somatosensory cortex, have also been implicated (Chamberlain 2009). These in turn may involve multiple neurotransmitter systems, including the monoaminergic (serotonergic, dopaminergic, noradrenergic), aminergic (glutamatergic, GABAergic) and others (opioid, cannabinoid).

SSRIs, such as fluoxetine and citalopram, are strongly serotonergic and have little effect on dopamine and noradrenaline reuptake. Inhibiting the reuptake of serotonin from the synaptic cleft leads to increased serotonergic neurotransmission, and clinical efficacy is observed at 70% to 80% serotonin receptor occupancy (Stahl 2008). TCAs, such as amitriptyline, also exhibit their effect through inhibiting the reuptake of catecholamines, such as noradrenaline and serotonin (Stahl 2008). Within this class, clomipramine exhibits predominantly serotonin reuptake inhibition, whilst other agents, such as desipramine, exhibit predominantly noradrenaline reuptake inhibition. SNRIs, such as venlafaxine, exhibit both serotonin and noradrenaline reuptake inhibition properties, increasing the activity of both of these monoamines in the brain.

In contrast, antipsychotics, such as olanzapine, are antagonists at certain dopamine and serotonin receptors, thereby modulating downstream effects of these monoamines (Stahl 2008). Mood stabilisers (e.g. lithium) and anticonvulsants, such as gabapentin and lamotrigine, invariably decrease glutamatergic neurotransmission or increase GABAergic activity, resulting in a generalised reduction of cerebral activity (Stahl 2008).

Glutamatergic dysfunction in an area of the reward circuitry, the nucleus accumbens, has been implicated in the pathogenesis of OCD (Chakrabarty 2005). This region is thought to play a role in other conditions for which impulse‐control and compulsive behaviours are predominant features, including TTM. The glutamate modulator NAC increases synaptic glutamate concentrations and stimulates inhibitory metabotropic glutamate receptors to restore glutamatergic homeostasis (Baker 2003a). Cannabinoid agonists, such as dronabinol, may also exert their effect by modulating glutamatergic neurotransmission in the basal ganglia and mesolimbic reward system (Grant 2011; Van der Stelt 2005).

Opioid antagonists, such as naltrexone, may be useful in the treatment of substance‐use disorders, possibly by inhibiting the sensation of reward associated with the addictive behaviour. It has been proposed that opioid antagonists may also be beneficial in the treatment of other disorders characterised by repetitive behaviours by modulating mesolimbic dopamine (Ikemoto 2010).

Inositol is an intracellular, carbocyclic sugar and a component of the phosphatidyl inositol second messenger system linked to serotonin, dopamine and glutamate metabolism (Camfield 2011). Silymarin is a milk thistle derivative with antioxidant and anti‐inflammatory properties, which may have a beneficial effect on dopamine functioning (Lu 2010).

Thus, it is possible that medications may target hypothesised mechanisms (e.g. altering the reward system), reducing hair‐pulling, or may be effective by addressing comorbid depression and OCD. Further work is needed to fully understand the mechanisms underlying TTM and how medication may be effectively utilised.

Why it is important to do this review

Previous reviews of pharmacological treatment for TTM concluded that no consistent and robust evidence supports the efficacy of any pharmacological agent in the treatment of TTM (Bloch 2007; Grant 2016; McGuire 2014; Rothbart 2013). As a number of additional trials have been published in recent years, an updated systematic review of medication for TTM is timely. A systematic synthesis of treatment data can also serve as the basis for future treatment guidelines, whilst assisting clinicians in effectively managing this disorder and identifying gaps in the current research base.

The authors updated the systematic review of RCTs of the pharmacotherapy of TTM, incorporating additional published trials, adding Summary of Findings tables and quality assessment according to GRADE, which have been added to Cochrane's standards since the initial publication. These were included as per Cochrane guidelines and using Cochrane software (Higgins 2011; Review Manager 2014).

Objectives

To assess the effects of medication for TTM in adults, children and adolescents compared with placebo or other medication.

Methods

Criteria for considering studies for this review

Types of studies

All published and unpublished RCTs, including studies with multiple treatment groups, cross‐over trials and cluster‐randomised controlled trials (cluster‐RCTs), were considered for inclusion in the review. We excluded pseudo‐randomised trials in the interest of minimising bias.

Types of participants

Participant characteristics

We included participants meeting the DSM‐III‐R (APA 1980) (or later) criteria for TTM in this review. We did not exclude trials consisting of participants who failed to satisfy the criteria of tension preceding the onset of hair‐pulling (criterion B) and pleasure, gratification or relief following hair‐pulling (criterion C), as people without these symptoms may nevertheless present with clinically significant hair‐pulling (Christenson 1991b; Du Toit 2001).

We applied no restrictions in terms of age, gender or ethnicity.

Comorbidities

We did not exclude participants with other comorbid psychiatric conditions.

Setting

We placed no restrictions on study setting.

Subsets of participants

Trials that included a subset of participants and met study inclusion criteria were also included in the analysis.

Types of interventions

Experimental interventions

For conducting searches and considering studies for inclusion in the review, we grouped specific medication interventions according to medication class. We included trials of medications in any of the following classes.

  • Antioxidants (e.g. silymarin).

  • Anticonvulsants (e.g. gabapentin, lamotrigine, levetiracetam, tiagabine, topiramate).

  • Antipsychotics (e.g. haloperidol, olanzapine, quetiapine, risperidone).

  • Benzodiazepines (e.g. alprazolam, bromazepam, clonazepam).

  • Cell signal transducers (e.g. inositol).

  • Glutamate modulators (e.g. N‐acetylcysteine (NAC)).

  • Monoamine oxidase inhibitors (MAOIs) (e.g. brofaromine, moclobemide, phenelzine).

  • Mood stabilisers (e.g. lithium).

  • Opioid antagonists (e.g. naltrexone).

  • Selective serotonin reuptake inhibitors (SSRIs) (e.g. citalopram, escitalopram, fluoxetine, fluvoxamine, paroxetine, sertraline).

  • Serotonin‐noradrenaline reuptake inhibitors (SNRIs) (e.g. venlafaxine).

  • Tricyclic antidepressants (TCAs) with predominantly SRI actions (e.g. clomipramine).

  • Other TCAs (e.g. amitriptyline, desipramine, imipramine).

Control conditions

Placebo or any agent in the medication classes listed above, or both.

Types of outcome measures

Primary outcomes

  • Treatment response: response to treatment determined using the Clinical Global Impressions‐Improvement item (CGI‐I, a widely‐used scale ranging from 1 = ‘very much improved’ to 7 = ‘very much worse’), used as a dichotomous measure of treatment response in which responders are defined as having a change item score of 1 = ‘very much improved’ or 2 = ‘much improved’ (Guy 1976). Where both dichotomous and continuous data for the CGI‐I were presented, we included only the categorical measure of ‘responders’ versus ‘non‐responders’. Where CGI‐I was not employed, we used other dichotomous measures of treatment response as reported in the original publication. Where no dichotomous measure was available, we report a continuous measure.

  • Reduction of TTM symptom severity: reduction in TTM symptom severity based on outcome measures such as the Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS) (Keuthen 1995), or similar, where available. The MGH‐HPS is a seven‐item, self‐report scale that rates urges to pull hair, actual amount of pulling, perceived control over behaviour and distress associated with hair‐pulling over the past seven days on a severity scale from 0 to 4 for each item (total scores range from 0 to 28, with higher scores reflecting greater illness severity). Clinician‐rated scales such as the National Institute for Mental Health ‐ Trichotillomania Severity and Impact Scales (NIMH‐TSS and NIMH‐TIS) are also reported where available. The NIMH‐TSS is a six‐item assessment, with total scores ranging from 0 to 20. Higher scores indicate greater severity or impairment. Where multiple scales were used within a study, we report on all for which data are available in the main text and data analysis. For the summary of findings tables, we prioritise reporting MGH‐HPS as a well‐validated scale for use in TTM, although it is a self‐report scale.

Secondary outcomes

  • Reduction of comorbid symptoms of depression: reduction in comorbid symptoms of depression quantified by the widely‐used Beck Depression Inventory scale (BDI: Beck 1961), Hamilton Depression Rating scale (HAM‐D: Hamilton 1960), or Montgomery‐Asberg Depression Rating Scale (MADRS: Montgomery 1979). The Hamilton Depression scale (HAM‐D) is a multiple‐item questionnaire with 17 to 29 items (depending on the version). People are rated on a 3‐ or 5‐point scale. A score of 0 to 7 is considered to be normal, and a score of 20 or higher, is moderate, severe or very severe. The Beck Depression Inventory (BDI) is a 21‐question multiple‐choice self‐report, one of the most widely‐used psychometric tests for measuring the severity of depression. A score of 0 to 9 indicates minimal depression, 10 to 18 mild depression, 19 to 29 moderate depression, and 30 to 63 severe depression. The MADRS is a 10‐item diagnostic questionnaire which psychiatrists use to measure the severity of depressive episodes in people with mood disorders. A higher MADRS score indicates more severe depression, and each item yields a score of 0 to 6. The overall score ranges from 0 to 60. Usual cutoff points are 0 to 6 ‐ normal/symptom absent; 7 to 19 – mild depression; 20 to 34 ‐ moderate depression; and above 34 – severe depression. Where multiple scales were used within one study, we report only one of them on a hierarchical basis, reporting HAM‐D if available, then BDI, MADRS or any other measure available. Where no data were available, and this was not an outcome of interest in the primary study, we do not report on this outcome.

  • Tolerability of treatment: tolerability of treatment using the following surrogate measures of medication acceptability. Where no data were available, and these were not outcomes of interest in the primary study, we do not report on these outcomes.

    • Dropouts due to adverse events: total proportion of people who withdrew from RCTs because of adverse events.

    • Common adverse events ( > 20%): most common drug‐related adverse events (> 20% of participants given the medication affected), as well as significant differences between medication and control groups in the occurrence of drug‐related adverse events. We do not report statistics for adverse events affecting less than 20% of participants but report the rates where available.

  • Quality of life ‐ functional disability: quality of life measures, such as the Quality of Life Enjoyment and Satisfaction Questionnaire (Q‐LES‐Q: Endicott 1993), as well as measures of functional disability, such as the Sheehan Disability Scale (SDS: Sheehan 1996, which includes subscales that assess impairment related to work, social life and family), were included when provided. The Sheehan Disability Scale is a composite of three self‐rated items designed to measure the extent to which three major sectors in an individual's life are impaired by panic, anxiety, phobic or depressive symptoms. The person rates the extent to which his or her work, social life or leisure activities, and home life or family responsibilities are impaired by his or her symptoms on a 10‐point visual analogue scale. The numerical ratings of 0 to 10 can be translated into a percentage if desired. The three items may be summed into a single dimensional measure of global functional impairment that ranges from 0 (unimpaired) to 30 (highly impaired). The Q‐LES‐Q is a lengthy, 90‐item questionnaire that assesses eight domains of life quality: physical health, subjective feelings, work, household duties, school, leisure activities, social relationships, and general activities. Where multiple scales were used within one study, we report only one of them on a hierarchical basis, reporting SDS if available; otherwise, we report Q‐LES‐Q or any other available measure. Where no data were available, and this was not an outcome of interest in the primary study, we do not report on this outcome.

Timing of outcome assessment

When studies reported response rates from baseline at various time points of the trial, treatment indices were subdivided as follows.

  • Early response – between one and four weeks; the time point closest to two weeks was given preference.

  • Acute phase treatment response – between 6 and 12 weeks; the time point as stated in the original study as the trial endpoint was given preference.

  • Follow‐up response – between four and six months; the time point closest to 24 weeks was given preference.

The acute phase treatment response – that is between 6 and 12 weeks from baseline – was our primary outcome of interest.

Search methods for identification of studies

We applied no date or language restrictions to the search for RCTs in any of the sources listed below.

Electronic searches

An information specialist with the Cochrane Common Mental Disorders (CCMD) group ran searches on the following databases and international trial registers. The search strategies are reported in Appendix 1.

  • Cochrane Common Mental Disorders Controlled Trials Register (CCMDCTR) (all available years) (archived database, current to June 2016).

  • Cochrane Central Register of Controlled Trials (CENTRAL; 2020, Issue 11) in the Cochrane Library (searched 26 November 2020).

  • MEDLINE Ovid (1946 to 26 November 2020).

  • Embase Ovid (1974 to 26 November 2020).

  • PsycINFO Ovid (from 1806 to 26 November 2020).

  • Proquest Dissertations and Thesis Database (PQDT) (all available years, searched 26 November 2020).

  • US National Institutes of Health Ongoing Trials Register ClinicalTrials.gov (www.clinicaltrials.gov; searched 26 November 2020).

  • World Health Organization International Clinical Trials Registry Platform (apps.who.int/trialsearch; searched 2 December 2019).

We ran additional searches on the following databases, using a single term 'trichotillomania', unless otherwise stated.

  • CINAHL EBSCO (Cumulative Index to Nursing and Allied Health Literature; 1982 to 21 January 2021).

  • LILACS (Latin American and Caribbean Health Science Information database; 1982 to 21 January 2021) (search: 'trichotillomania' or 'tricotilomania').

  • African Index Medicus (all available years, searched 21 January 2021).

  • Informit Health Collection (Australia) (1970 to 2020) (searched 21 January 2021).

  • Index Medicus for the Eastern Mediterranean Region (1984 to 2020) (searched 21 January 2021).

  • IndMed (India) (1985 to 2020) (searched 21 January 2021).

  • KoreaMed (1997 to 2020) (searched 21 January 2021).

  • Ukraine and the Russian Federation – Panteleimon (1998 to 2020) (searched 21 January 2021).

  • Western Pacific Region Index Medicus (all available years, searched 21 January 2021).

We also ran an update of the international trial registers at this time.

  • US National Institutes of Health Ongoing Trials Register ClinicalTrials.gov (www.clinicaltrials.gov; searched 21 January 2021);

  • World Health Organization International Clinical Trials Registry Platform (apps.who.int/trialsearch; searched 21 January 2021).

Searches conducted for the previous version of the review, Rothbart 2013, are reported in Appendix 2.
 

Searching other resources

Reference lists

We scanned the bibliographies of all identified trials for additional studies.

Correspondence

We obtained published and unpublished trials from key researchers, as identified by the frequency with which they are cited in the bibliographies of RCTs and open‐label studies.

Grey literature searches

One review author (JH) performed a search of the following sources of grey literature, theses databases and conference abstracts (all available years to 21 January 2021).

Theses databases

Conference abstracts

We also searched the following pharmaceutical industry trial registers: AstraZeneca; Bristol‐Myers Squibb; Eli Lilly; GlaxoSmithKline; Novartis; Roche and Pfizer/Wyeth.

Finally, we conducted a forwards citation search on the Web of Science (reports of included studies) to identify any additional research.

Data collection and analysis

We used Review Manager 5 (RevMan 5) to perform all analyses reported in this review (Review Manager 2014).

Selection of studies

Two review authors (JH, TW) independently examined the titles and abstracts of all studies obtained through the search strategy. The same two review authors obtained and independently assessed the full texts of relevant articles that appeared to meet the inclusion criteria. Each review author then independently applied the full eligibility criteria for inclusion in the review to the full‐text articles. Any conflicts of opinion were discussed, and arbitrated by another review author (DJS) if necessary, until consensus was reached.

Data extraction and management

Two review authors (JH, TW) independently collected data. We resolved any disagreements regarding the data collection procedures through discussion with a third review author (DJS). We created digital data extraction sheets for the purpose of manually recording descriptive information, summary statistics of the outcomes, quality scale ratings and associated commentary. We used Google Forms to set up a data extraction tool to streamline data extraction and entry directly into Excel (example at forms.gle/zqgpAics3PB6q7ud6). A script was written in Python using the Spyder IDE (version 3.3.6) to aid extraction of trial data housed as XML on ClinicalTrials.gov (www.clinicaltrials.gov). Where available, we compared trial information to published data. Once collated, we entered data into Review Manager 5 (RevMan 5) software, which was used to conduct the meta‐analysis. We contacted investigators by email to try to obtain missing information. No reports required translation.

We collected the following information from each included study.

  • Description of the trial, including the primary researcher, year of publication, trial protocol identification, number of centres involved, country where the research was conducted and the source of funding.

  • Characteristics of the intervention, including the number of participants randomly assigned to the treatment and control groups, the total number of dropouts per group and the number who dropped out because of adverse effects.

  • Characteristics of trial methodology, including the recruitment process, diagnostic (e.g. DSM‐IV (APA 2000)) and exclusionary criteria employed, the screening instrument used (e.g. the Structured Clinical Interview for DSM‐IV (SCID) (Spitzer 1996)) for the primary and comorbid diagnoses, the presence of comorbid major depressive disorder (MDD), the use of a placebo run‐in, whether a minimal severity criterion was employed and the length of the study.

  • Characteristics of samples, including total number of participants, gender distribution and age distribution, mean age at diagnosis with TTM, mean length of time since diagnosis with TTM, whether participants have been treated with the medication in the past (treatment naivety), the number of participants in the sample with psychiatric comorbidities and the baseline severity of TTM, as assessed by the primary outcome measure reported in the trial or another commonly employed scale.

  • Characteristics of the drug, including the drug class, dose, route and frequency of drug administration throughout all trial phases, the duration of the trial and details of any washout period or placebo run‐in where applicable.

  • Characteristics of the control measure, including type of control utilised and methods for concealing the placebo where applicable.

  • Outcome measures employed (primary and secondary) and summary continuous (means and standard deviations) and dichotomous (number of responders) data. We included additional information, such as whether data reflected the intention‐to‐treat (ITT) with last observation carried forward (LOCF) or completer/observed cases (OC) sample, and the minimal period required for inclusion of participants in the LOCF analyses. We recorded other methods of estimating the outcome for participants who dropped out of the study, such as the mixed effects (ME) model.

Main comparisons

We compared the following medications, grouped by class, against placebo or other active agents, for treating TTM in adults, children and adolescents.

  • Antioxidants (e.g. silymarin).

  • Antipsychotics (e.g. olanzapine).

  • Cell signal transducers (e.g. inositol).

  • Glutamate modulators (e.g. N‐acetylcysteine).

  • Opioid antagonists (e.g. naltrexone).

  • SSRIs (e.g. fluoxetine, sertraline).

  • TCAs with predominantly SRI actions (e.g. clomipramine).

We planned the following comparisons and grouped specific pharmacological interventions according to medication class based on the included studies.

Comparison 1: antioxidants versus placebo in adults.

Comparison 2: antioxidants versus placebo in children and adolescents.

Comparison 3: antipsychotics versus placebo in adults.

Comparison 4: cell signal transducers versus placebo in adults.

Comparison 5: glutamate modulators versus placebo in adults.

Comparison 6: glutamate modulators versus placebo in children and adolescents.

Comparison 7: opioid antagonists versus placebo in adults.

Comparison 8: SSRIs versus placebo in adults.

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults.

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults.

Assessment of risk of bias in included studies

Two review authors (JH, TW) independently examined the components of each included trial for risk of bias using a standard form. This form included information on sequence generation, allocation concealment, blinding (participants, personnel and outcome assessor), incomplete outcome data, selective outcome reporting and other sources of bias. We assessed the methodological components of the trials as having a low, high or unclear risk of bias, as per the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011, hereafter referred to as the Cochrane Handbook). When differences arose, we resolved these through discussion with a third review author (DJS).

Sequence generation

  • Low risk: investigators described a random component in the sequence generation process, such as the use of a random number table, coin tossing, cards or envelope shuffling.

  • High risk: investigators described a non‐random component in the sequence generation process, such as the use of odd or even date of birth, algorithm based on the day or date of birth, or hospital or clinic record number.

  • Unclear: insufficient information was provided to permit judgement of the sequence generation process.

Allocation concealment

  • Low risk: participants and investigators enrolling participants could not foresee assignment (e.g. central allocation or sequentially numbered, opaque, sealed envelopes). Measures were taken to ensure placebo unidentifiable from intervention (e.g. masking of smell of drug and placebo).

  • High risk: participants and investigators enrolling participants could foresee upcoming assignment (e.g. open random allocation schedule, such as a list of random numbers, or envelopes that were unsealed or non­opaque or were not sequentially numbered). Placebo was distinct from intervention drug and no attempt was made to conceal this (e.g. clear versus opaque syrup used).

  • Unclear: insufficient information was provided to permit judgement of allocation concealment, or the method was not described.

Blinding

  • Low risk: blinding of participants, key study personnel and outcome assessors were described, and it is unlikely that blinding could have been broken; or lack of blinding was described in a situation where non‐blinding was not likely to introduce bias.

  • High risk: no blinding or incomplete blinding was described, and the outcome was likely to be influenced by lack of blinding.

  • Unclear: insufficient information was provided to permit judgement of adequacy or otherwise of the blinding.

Incomplete outcome data

  • Low risk: no outcome data were missing, reasons for missing outcome data were unlikely to be related to true outcome, or missing outcome data were balanced in number across groups. Intention‐to‐treat analysis was employed.

  • High risk: reason for missing outcome data was likely to be related to the true outcome, with imbalance in numbers across groups or in reasons for missing data. Intention‐to‐treat analysis was not employed, and no explanation given.

  • Unclear: reporting of attrition or exclusions was insufficient.

Selective outcome reporting

  • Low risk: a protocol that clearly stated the primary outcome as the same as in the final trial report was available.

  • High risk: the primary outcome differs between the protocol and the final trial report.

  • Unclear: no trial protocol was available, or reporting was insufficient to determine whether selective reporting was present.

Other sources of bias

  • Low risk: no evidence suggested bias from other sources.

  • High risk: potential bias from other sources was present (e.g. early stopping of trial, fraudulent activity, extreme baseline imbalance or bias related to specific study design).

  • Unclear: insufficient information was provided to permit judgement of adequacy or otherwise of other forms of bias.

Measures of treatment effect

Dichotomous data

We calculated the risk ratio (RR) and the 95% confidence interval (CI) for the dichotomous outcomes of interest, including treatment response (CGI‐I or related measure) and dropouts due to adverse events. We also calculated the number needed to treat for an additional beneficial outcome (NNTB). NNTB is defined as the inverse of the absolute risk difference due to the medication intervention. In this review, we use NNTB to indicate the number of participants who require treatment with medication, relative to a control, before a single additional participant in the medication group responds to treatment. As the outcome measured is favourable, a negative NNT was defined as the NNTB.

Continuous data

We calculated effect size as mean difference (MD) for continuous summary data where a single outcome scale was used to measure the outcome of interest within a single study or across multiple studies (e.g. MGH‐HPS, NIMH‐TSS or related measure). For primary outcomes, where multiple scales were used within a single study, we report all as MD. Where multiple scales were employed across multiple studies for a single primary outcome, we planned to calculate the standardised mean difference (SMD). However, this was not required. For secondary outcomes where multiple scales were applied, we selected a single appropriate scale in a hierarchical manner and report the MD (e.g. HAM‐D, SDS or related measure).

Skewed data

When evidence indicated that data were skewed, we planned to obtain individual participant data (when possible) for the purpose of normalising the data through the use of log transformation techniques. If this proved unsuccessful, we planned to exclude those studies that provided skewed data from the analysis. For the purposes of this review, the following constituted evidence of skewness: cases in which the difference between the observed mean and the lowest possible value or the highest possible value on the scale is less than twice as large as the standard deviation (Altman 1996), or cases in which data are reported as skewed by the authors.

Unit of analysis issues

Studies with multiple treatment groups

We did not include any studies with multiple treatment groups in this review. In future updates of the review, if trials with three or more arms are identified, it may be appropriate to do a multi‐arm trial analysis, wherein the placebo group would be split and shared between two or more groups with smaller sample sizes. In this way, the two or more intervention groups can be analysed as subgroups (Higgins 2011).

In our analyses, for most comparisons, only one study provided data on primary and secondary outcomes. For continuous outcomes, in order to understand the results for each measure used within one trial, and where multiple sclaes were used, these were displayed in one meta‐analysis. For these analyses, we have not displayed totals, as these would be misleading.

Cross‐over trials

We included cross‐over trials in the calculation of outcomes of interest only: (1) when it was possible to extract medication and placebo or comparator data from the first treatment period; or (2) when inclusion of data from both treatment periods was justified by a washout period of sufficient duration as to minimise the risk of carry‐over effects. We defined an adequate washout period in accordance with clinical practice as at least two weeks for all agents, except for fluoxetine, for which a minimum washout period of four weeks was required, given the long plasma half‐life of this agent. We included cross‐over trials that lacked a washout period if the agents compared were of the same class and had similar properties. For trials in which the washout period was regarded as adequate, we included data from both periods when it was possible to determine the standard error of the mean difference in response between groups (Elbourne 2002). We obtained the summary statistics required to derive the standard error from the trial report. In the future, for trials for which this information is missing, we plan to impute the summary statistics by averaging the relevant statistic from other included cross‐over trials with comparable control conditions.

Cluster‐randomised trials

We did not include any cluster‐RCTs in this review. In future updates of the review, if cluster‐RCTs are identified, we would apply an intraclass correlation (ICC) for the sample to account for the effect of clustering. We would use the ICC reported in the publication, or, if necessary, we would contact study authors to request this information. If we were unable to obtain this information, we would calculate an ICC estimate using the average of the ICCs obtained from the other studies included in the analysis. We would undertake the analysis by using generic inverse variance (GIV).

Dealing with missing data

We conducted all analyses as ITT. We used the total number of participants randomly assigned to the different comparison groups as the denominator in comparisons of treatment response. Only data from trials that provided information on the original group size (before dropouts) were eligible for inclusion in the analyses of treatment response. We gave preference to the inclusion of summary statistics for continuous outcome measures derived from mixed effects (ME) models, followed by last observation carried forward (LOCF) and observed cases (OC) summary statistics (in that order). This is in line with evidence that ME methods are more robust to bias than LOCF analyses (Verbeke 2000).

Assessment of heterogeneity

For trials in which the methods and clinical characteristics were sufficiently homogeneous that they could be combined, we assessed statistical heterogeneity of treatment response and reduction of symptom severity visually from the forest plot. This helped us to determine whether differences between the results of trials were greater than would be expected by chance alone. We assessed heterogeneity by using the Chi2 test of heterogeneity. If the Chi2 test had a P value of less than 0.10, we interpreted this as evidence of heterogeneity, given the low power of the Chi2 statistic when the number of trials is small (Deeks 2021).

In addition, we used the I2 heterogeneity statistic, as reported by RevMan 5, to test the robustness of the Chi2 statistic to differences in the number of trials included in the groups compared within each subgroup analysis (Higgins 2003).

Thresholds for the interpretation of I2 can be misleading because the importance of inconsistency depends on several factors. A rough guide for interpretation was followed:

  • 0% to 40%: may not be important;

  • 30% to 60%: may represent moderate heterogeneity;

  • 50% to 90%: may represent substantial heterogeneity;

  • 75% to 100%: may represent considerable heterogeneity.

We assessed differences on continuous measures in medication efficacy between these groups by means of Deeks’ stratified test of heterogeneity (Deeks 2001). This method subtracts the sum of the Chi2 statistics available for each of the subgroups in the study from the Chi2 statistic available for all of the trials, to obtain a measure (Qb) of heterogeneity between groups. We determined differences in treatment response on the CGI‐I by noting whether the confidence intervals for the effect sizes of the subgroups overlap. This method was chosen in preference to the stratified test because of inaccuracies in the calculation in RevMan 5 of the Chi2 statistic for dichotomous measures (Deeks 2021).

Assessment of reporting biases

Publication is not necessarily related to study quality, and indeed publication may imply certain biases (Dickersin 1992; Song 2000). We planned to assess small‐sample effects (including publication bias) through visual inspection of a funnel plot of treatment response. This is possible, however, only when more than 10 studies are included in the funnel plot. We did not carry out this assessment in this review due to insufficient studies within comparisons.

Data synthesis

In conducting a meta‐analysis, we obtained categorical and continuous treatment effects from a random‐effects model (the random‐effects model includes both within‐study sampling error and between‐studies variation in determining the precision of the confidence interval around the overall effect size, whereas the fixed‐effect model takes only within‐study variation into account). The outcomes are expressed in terms of an average effect size, as well as by means of 95% confidence intervals.

In future updates, if appropriate, we may consider using 'multiple‐treatment meta‐analyses' (MTM) methodology to compare and analyse intervention groups across studies. This method relies on the strong assumption that studies of different comparisons are similar in all ways other than the interventions being compared (Higgins 2011).

Subgroup analysis and investigation of heterogeneity

We planned to undertake subgroup analyses to assess the degree to which methodological differences between trials might have systematically influenced differences observed in primary treatment outcomes. The a priori subgroups that we planned to explore included the following.

  • Involvement of participants from a single centre or from multiple centres. Single‐centre trials may be associated with lower sample size but less variability in clinician ratings (Youssef 2008).

  • Whether trials were industry‐funded. In general, published trials that are sponsored by pharmaceutical companies appear more likely to report positive findings than trials that are not supported by for‐profit companies (Als‐Nielsen 2003; Baker 2003b).

In addition, we planned to use the following criterion to assess the extent of clinical sources of heterogeneity.

  • Whether the sample included participants diagnosed with major depressive disorder (MDD). Such an analysis might assist in determining the extent to which the efficacy of a medication used in treating TTM is independent from its ability to reduce symptoms of depression—an important consideration given the classification of many of these medications as antidepressants.

We did not include enough studies to permit subgroup analysis or investigation of the clinical sources of heterogeneity.

Sensitivity analysis

Sensitivity analyses determine the robustness of the review authors’ conclusions to methodological assumptions made in conducting the meta‐analysis. There were not enough included studies to permit sensitivity analyses. However, in future updates, we plan to conduct sensitivity analyses to determine whether treatment response varies as a function of:

  • the use of treatment response versus non‐response as an outcome statistic. This comparison may be necessary in the light of evidence that treatment response may result in less consistent outcome statistics than non‐response (Deeks 2002), when the control group event rate is higher than 50%. This sensitivity analysis would accordingly be performed only if most trials report a control group event rate higher than 50%;

  • the exclusion of participants who were lost to follow‐up (LTFU). We planned to determine this through a 'worst case/best case' scenario (Deeks 2008). In the worst case, all missing data for the treatment group are recorded as non‐responders, whereas in the best case, all missing data for the control group are treated as non‐responders. Should conclusions regarding treatment efficacy not differ between these two comparisons, it can be assumed that missing data in trial reports do not have a significant influence on outcome;

  • the exclusion of results based on LOCF or OC;

  • the exclusion of cross‐over trials;

  • the exclusion of cluster‐randomised trials; or

  • varying ICCs in cluster‐randomised trials.

Summary of findings and assessment of the certainty of the evidence

We compiled summary of findings tables to summarise the evidence presented for the outcomes of treatment response, reduction of TTM symptom severity and tolerability of treatment (e.g. dropouts due to adverse events). These outcomes are displayed in the summary of findings tables for all comparisons. Where multiple scales were reported for reduction of TTM symptom severity, we report only a single outcome measure for each comparison in our summary of findings tables, prioritising MGH‐HPS where available, but report on all outcome scales used within the text and data analysis sections of this review. We summarised the findings and graded the certainty of the evidence, in a fixed format using GRADEpro software (GRADEpro GDT).

We classified reasons for downgrading the certainty of the evidence as ‘serious’ (downgrading the certainty rating by one level) or ‘very serious’ (downgrading the certainty rating by two levels). We graded the certainty of evidence based on these five factors:

  • limitations in the design and implementation of the trial;

  • indirectness of evidence;

  • unexplained heterogeneity or inconsistency of results;

  • imprecision of results;

  • high probability of publication bias.

With regards to grading the certainty of the evidence, for risk of bias, we downgraded by one level for every identified source of potential bias. For inconsistency, we downgraded by zero levels if heterogeneity amongst studies was less than 30%, by one level if heterogeneity was between 30% and 60%, and by two levels if heterogeneity was greater than 60%. For indirectness, we downgraded based on judgement (four factors). Downgrading for indirectness was based on any concerns related to differences in the study populations, differences in interventions, differences in outcome measures (surrogate outcomes) and indirect comparisons. We did not downgrade due to publication bias as there were insufficient studies to generate funnel plots (Schünemann 2013).

For imprecision, we downgraded by two levels for a 95% confidence interval that crossed the significance threshold (0 for SMD and MD, 1 for RR) and by zero to two levels depending on the sample size. Sample size thresholds for downgrading were determined using power analysis for 1 study and SMD = 0.3 ‐ 1, tested using both fixed‐effect and random‐effects models. A total of 47 participants were required to detect a change of SMD = 1 at 80% power with a random‐effects model (low heterogeneity). Using a fixed‐effect model, 36 participants are required. For 50% power, 17 participants are required for fixed‐effect and 23 are required for random‐effects model analyses. To detect an effect size of 0.3, a sample size of 469 is required to reach 80% power using a random‐effects model and 353 are needed using a fixed‐effect model. The thresholds used for downgrading the certainty of the evidence based on pooled sample size were: 0 levels if more than 400 participants; ‐1 level if 50 to 400 participants; and ‐2 levels if less than 50 participants in the analysis.

We classified the overall certainty in the evidence (or quality of the evidence) for each comparison according to the following categories.

  • High certainty: further evidence is unlikely to change our confidence in the estimate of effect.

  • Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.

  • Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.

  • Very low certainty: we are very uncertain about the estimate.

Results

Description of studies

Results of the search

Our searches yielded 2458 records. After examination of their titles and abstracts, we obtained the full texts of 22 studies to analyse them for inclusion. Twelve studies met the inclusion criteria for the review (Figure 1).


PRISMA flow diagram

PRISMA flow diagram

We attempted to contact the principal investigators of 10 of the 12 included studies to obtain or verify information (eight people, as Christenson authored two studies (Christenson 1991a; Christenson 1994), and Grant was the primary contact person for four studies (Grant 2009; Grant 2014; Grant 2019; Leppink 2017)). We were successful in contacting and obtaining information from six of the eight study authors.

Included studies

See Characteristics of included studies.

Design

Of the 12 studies identified as eligible for the review, all were RCTs. Eleven trials were conducted in the United States and one in Canada (Van Ameringen 2010). Only two trials included children and adolescents under 18 years old (Bloch 2013Grant 2019). Eleven trials were conducted with adult participants aged 18 to 65. Four of the trials used a cross‐over design (Christenson 1991aGrant 2019Streichenwein 1995Swedo 1989), and eight trials used a parallel‐group design (Bloch 2013Christenson 1994Dougherty 2006Grant 2009Grant 2014Leppink 2017Ninan 2000Van Ameringen 2010). The four cross‐over trials were 17 weeks, 13 weeks, 27 weeks and 10 weeks in duration, respectively. Of the parallel‐group trials, one was 6 weeks in duration, one was 8 weeks in duration, one was 9 weeks in duration, one was 10 weeks in duration, and four were 12 weeks in duration. All of the studies were published in English language journals, with the exception of one (Christenson 1994), which was presented as a conference abstract. Four studies were funded by pharmaceutical companies (Dougherty 2006Ninan 2000Streichenwein 1995Van Ameringen 2010).

Sample sizes

The eleven studies conducted with adults involved a total of 298 participants with a mean sample size of 27 participants per trial, a median of 24 and a range from the smallest sample size of 13 to the largest of 51. The single study exclusively in children and adolescents included 39 participants (Bloch 2013). A single study was conducted in adults, children and adolescents, and included 22 participants: 18 adults and 4 children and adolescents (Grant 2019). These adult participants are included in the total reported above.

Setting

All studies were single‐centre trials, and all participants were seen on an outpatient basis.

Participants

Nine of the 12 trials report using DSM‐III‐R (or later) criteria to select participants (Bloch 2013Christenson 1991aDougherty 2006Grant 2009Grant 2014Grant 2019Leppink 2017Ninan 2000Van Ameringen 2010). The remaining three trials do not report the specific criteria employed in participant selection (Christenson 1994Streichenwein 1995Swedo 1989). Three trials did not require DSM‐III‐R and ‐IV criteria B and C for inclusion in the trials (i.e. a sense of tension before and a sense of relief after hair‐pulling) (Bloch 2013Christenson 1991aGrant 2009). Of the 10 trials that reported the gender of participants, nine reported the proportion of female participants as 75% to 100%, reflecting female predominance in TTM (Bloch 2013Christenson 1991aGrant 2009Grant 2014Grant 2019Leppink 2017Ninan 2000Streichenwein 1995Swedo 1989). The mean age of adult participants in the eight trials that reported this variable was between 28 and 40 years (Christenson 1991aGrant 2009Grant 2014Leppink 2017Ninan 2000Streichenwein 1995Swedo 1989Van Ameringen 2010). The average age of participants in the trial on children and adolescents was 13 years (Bloch 2013). The mean age of participants in the trial conducted in children, adolescents and adults was 28.1 years (Grant 2019).

Lifetime prevalence rates of comorbid psychiatric conditions were reported in seven trials in adults. Rates of major depressive disorder or a history of major depressive disorder ranged from 15.8% to 46.2% in four trials (Christenson 1991aGrant 2009Leppink 2017Swedo 1989); and rates of anxiety disorders ranged from 20.0% to 75.0% in six trials (Christenson 1991aGrant 2009Leppink 2017Streichenwein 1995Swedo 1989Van Ameringen 2010). Two studies reported rates of 'another impulse‐control disorder' as 20.0% and 36.0%, respectively (Grant 2009Van Ameringen 2010). The same two studies reported rates of eating disorders of 4.0% and 2.0%, respectively. One study reported rates of skin picking disorder as 34.2%, attention‐deficit hyperactivity disorder (ADHD) as 2.6%, and obsessive‐compulsive disorder (OCD) as 2.6% (Leppink 2017). One study reported a significant rate of drug and alcohol use among participants (30.8%; Swedo 1989), and one article stated that 52.9% of their participants had psychiatric comorbidities, although no further details were available (Grant 2014). The study in children and adolescents reported rates of depression as 33.3%, anxiety as 23.1%, ADHD as 10%, tic disorder as 7.7%, OCD as 5.1%, and skin picking disorder as 2.6% (Bloch 2013). The study conducted in children, adolescents and adults reported current psychotropic medicine use as 35% (adults only = 25%; children and adolescents only = 75%), current ADHD as 25% (adults only = 18.8%; children and adolescents only = 50%), current depression as 35% (adults only = 25%; children and adolescents only = 75%), current anxiety as 30% (adults only = 18.8%; children and adolescents only = 75%), current nail‐biting as 25% (adults only = 25%; children and adolescents only = 25%) and current skin picking as 60% (adults only = 50%; children and adolescents only = 100%) (Grant 2019).

Interventions

The 11 studies in adults included three studies of SSRIs (two fluoxetine (Christenson 1991aStreichenwein 1995), and one sertraline (Dougherty 2006)); two of TCAs with predominantly SRI actions (clomipramine (Ninan 2000Swedo 1989)); one of an antipsychotic (olanzapine (Van Ameringen 2010)); one of a glutamate modulator (NAC (Grant 2009)); two of an opioid antagonist (naltrexone (Christenson 1994Grant 2014)); one of a carbocyclic sugar involved in cell signal transduction (inositol (Leppink 2017)); and one of a flavonoid derived from milk thistle extract with antioxidant properties (silymarin (Grant 2019)). The single study exclusively in children and adolescents examined a glutamate modulator (NAC (Bloch 2013)). A placebo comparison group was employed in all but one trial, which involved an active agent comparator (Swedo 1989). Of the four trials employing a cross‐over design (Christenson 1991aGrant 2019Streichenwein 1995Swedo 1989), two involved a five‐week washout period before cross‐over between fluoxetine and placebo (Christenson 1991aStreichenwein 1995). In Swedo 1989, a washout period was not employed, as desipramine was used as an active control and has similar properties to the intervention (clomipramine); therefore, a washout period was not deemed necessary. In Grant 2019, a one‐week washout period was employed between intervention (silymarin) and placebo arms. All trials employed gradual dose progression, except for one of the naltrexone trials (Christenson 1994), for which a constant dose was given throughout the trial. All interventions were oral medications or placebo, taken by participants at home.

Outcomes

In the adult studies, seven trials employed the Clinical Global Impression – Improvement item (CGI‐I) Scale to measure treatment response (Dougherty 2006Grant 2009Grant 2014Grant 2019Leppink 2017Ninan 2000Van Ameringen 2010); two trials employed an untitled scale that measured five aspects of self‐reported TTM severity (Christenson 1991aStreichenwein 1995); six trials employed the validated National Institute of Mental Health (NIMH) Trichotillomania Severity Scale (TSS) and the Trichotillomania Impairment Scale (TIS) (Christenson 1994Grant 2014Grant 2019Leppink 2017Ninan 2000Swedo 1989); six trials employed the Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS) (Dougherty 2006Grant 2009Grant 2014Grant 2019Leppink 2017Van Ameringen 2010); two trials employed the Psychiatric Institute Trichotillomania Scale (PITS) (Dougherty 2006Grant 2009); one trial employed the Trichotillomania Impact Scale (TTMIS) (Dougherty 2006); and one trial employed the Yale‐Brown Obsessive‐Compulsive Scale for TTM (Van Ameringen 2010).

Secondary outcome measures employed in adult studies were the Hamilton Rating Scale for Depression (HAM‐D) (Christenson 1991aDougherty 2006Grant 2009Grant 2014Grant 2019Leppink 2017Streichenwein 1995), the Hamilton Rating Scale for Anxiety (HAM‐A) (Grant 2009Grant 2014Grant 2019Leppink 2017), the Beck Depression Inventory (BDI) (Christenson 1991aDougherty 2006Ninan 2000Streichenwein 1995Van Ameringen 2010), the Beck Anxiety Inventory (BAI) (Dougherty 2006Van Ameringen 2010), the State‐Trait Anxiety Inventory (STAI) (Ninan 2000), the NIMH Global Assessment Scales for Depression and Anxiety (NIMH‐GASD) (Swedo 1989), the Quality of Life Enjoyment and Satisfaction Questionnaire (Q‐LES‐Q) (Dougherty 2006Van Ameringen 2010), the Quality of Life Inventory (QoLI) (Grant 2009Grant 2014Leppink 2017), and the Sheehan Disability Scale (SDS) (Grant 2009Grant 2014Grant 2019Leppink 2017Van Ameringen 2010).

The studies in children and adolescents used the CGI‐I to measure treatment response (Bloch 2013Grant 2019). In the same studies, the MGH‐HPS, the NIMH‐TSS and the Trichotillomania Scale for Children–Child and Parent versions (TSC‐C,P) were used to measure symptom severity. The Children’s Depression Inventory (CDI) was used to measure symptoms of depression in one of the studies (Bloch 2013). HAM‐A, HAM‐D and SDS were applied in the other study as secondary outcome measures (Grant 2019).

Excluded studies

See Characteristics of excluded studies.

We excluded 10 studies for the following reasons: non‐RCT design (Black 1992; Chamberlain 2010; Epperson 1996; Golubchik 2011; Ninan 1998; Riley 1993; Stein 1995; Stein 1997); waiting‐list control group instead of placebo (Van Minnen 2003); and dietary intervention, not pharmacotherapy (Dufour 2010).

Ongoing studies

We identified four ongoing studies. Three ongoing studies were identified with protocols on ClinicalTrials.gov, and one study on the Iranian Registry of Clinical Trials (en.ICRT.ir).

Of the three identified on ClinicalTrials.gov, one study investigated NAC, glutathione levels and compulsivity in anorexia nervosa and other disorders characterised by compulsive behaviour, including TTM (NCT02794389; completed, no results posted; NCT02794389). The second study is investigating dronabinol, a synthetic cannabinol, in TTM and other body‐focused repetitive behaviours (NCT03530800; recruiting; NCT03530800). The last study is focusing on an experimental drug, SXC‐2023, which may affect glutamatergic dysfunction and oxidative stress response (NCT03797521; active, recruitment completed; NCT03797521). The study on IRCT.ir investigates the individual and combined effects of habit‐reversal therapy (HRT) and citalopram in TTM (IRCT20181009041282N2; active, not recruiting; IRCT20181009041282N2).

Studies awaiting classification

One study is awaiting publication of phase II trial results, which was conducted under randomised, placebo‐controlled conditions (Ninan 1998). However, we could not find a reference for the phase II results of this trial, and therefore have excluded the publication of phase I results under ‘Excluded studies’.

Risk of bias in included studies

Full details of the determination of risk of bias can be found in Characteristics of included studies and in Figure 2 and Figure 3.


Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies


Risk of bias summary: review authors' judgements about each risk of bias item for each included study

Risk of bias summary: review authors' judgements about each risk of bias item for each included study

Allocation

Random sequence generation

We rated the risk of bias arising from the method of generation of the allocation sequence as low in ten studies (Christenson 1991a; Christenson 1994; Dougherty 2006; Grant 2009; Grant 2014; Grant 2019; Leppink 2017; Streichenwein 1995; Swedo 1989; Van Ameringen 2010). These studies reported generating the sequence by computer or by a random number table, or such information was obtained from the first author. Ninan 2000 and Bloch 2013 did not disclose a method of randomisation; therefore, the presence of selection bias is unclear for these studies.

Allocation concealment

We rated the risk of bias arising from the method of allocation concealment as low in ten studies (Bloch 2013; Christenson 1991a; Christenson 1994; Dougherty 2006; Grant 2009; Grant 2019; Leppink 2017; Streichenwein 1995; Swedo 1989; Van Ameringen 2010). These studies reported the use of central allocation (e.g. pharmacy‐controlled allocation), or this information was obtained from the first author. Ninan 2000 and Grant 2014 did not disclose a method of allocation; therefore, the presence of selection bias is unclear for these studies.

Blinding

Blinding of participants and personnel (performance bias)

We rated the risk of bias arising from lack of blinding of participants and personnel as low for 11 of the 12 studies. Most studies reported using a placebo or other form of control that was identical in appearance to the intervention. If not reported, blinding of participants was confirmed by correspondence with the author (Christenson 1991a; Christenson 1994; Dougherty 2006; Grant 2009; Grant 2014; Grant 2019; Leppink 2017; Streichenwein 1995; Swedo 1989; Van Ameringen 2010). Bloch 2013 disclosed quadruple blinding was employed and significant effort was taken to match the placebo to NAC in appearance and smell, thus performance bias was rated as low. Ninan 2000 did not disclose a method for blinding participants, but stated a double‐blind study design; therefore, the presence of performance bias is unclear for this study.

Blinding of outcome assessors (detection bias)

We rated the risk of bias arising from lack of blinding of outcome assessors as low for all studies. Most studies reported blind outcome assessment; if not, this information was obtained from the first author (Bloch 2013; Christenson 1991a; Christenson 1994; Dougherty 2006; Grant 2009; Grant 2014; Grant 2019; Leppink 2017; Ninan 2000; Streichenwein 1995; Swedo 1989; Van Ameringen 2010).

Incomplete outcome data

We rated risk of attrition bias as low in eight trials which employed ITT analysis or in which attrition rates were not differentially distributed between intervention and control groups, or both (Bloch 2013; Christenson 1991a; Grant 2009; Grant 2014; Grant 2019; Leppink 2017; Swedo 1989; Van Ameringen 2010). We rated the risk of attrition bias as high in three trials, in which attrition was greater than 10% overall and/or ITT analysis was not employed, and/or attrition rates were differentially distributed between intervention and control groups (Dougherty 2006; Ninan 2000; Streichenwein 1995). Dropout rates were not reported for the Christenson 1994 trial, and therefore we assessed this trial as unclear risk of bias.

Selective reporting

We obtained trial protocols for six trials, with four trials reported additional outcomes in their publication compared to their protocol (Bloch 2013; Grant 2009; Grant 2014; Leppink 2017). All outcomes from four of the protocols were reported in the publications of the studies. Therefore, we rated the risk of reporting bias for these trials as low (Bloch 2013; Grant 2009; Grant 2014; Leppink 2017). One study reported an outcome in the protocol, but not in the publication (Grant 2019). However, the results would not change the conclusion, and therefore we rated the risk of reporting bias as low (Grant 2019). The other trial protocol obtained revealed no evidence for reporting bias and was also rated as low (Van Ameringen 2010). We did not obtain trial protocols for the remaining six trials, and therefore, we rated the risk of reporting bias as unclear for those trials (Christenson 1991a; Christenson 1994; Dougherty 2006; Ninan 2000; Streichenwein 1995; Swedo 1989).

Other potential sources of bias

There were few other potential sources of bias. Of note, most studies reported a marked female predominance in percentage of participants, however the effect of this is unclear (Bloch 2013; Christenson 1991a; Dougherty 2006; Grant 2009; Grant 2014; Grant 2019; Leppink 2017; Ninan 2000; Streichenwein 1995; Swedo 1989; Van Ameringen 2010). A few of the studies also reported either industry‐funding (Dougherty 2006; Streichenwein 1995; Van Ameringen 2010), medication provided by the pharmaceutical industry (Dougherty 2006; Ninan 2000; Streichenwein 1995), or had authors who worked as consultants for pharmaceutical companies (Grant 2009; Leppink 2017). The relevance of this with regards to potential bias was rated as unclear.

Effects of interventions

See: Summary of findings 1 Antioxidants versus placebo for trichotillomania in adults; Summary of findings 2 Antioxidants versus placebo for trichotillomania in adolescents; Summary of findings 3 Antipsychotics versus placebo for trichotillomania in adults; Summary of findings 4 Cell signal transducers versus placebo for trichotillomania in adults; Summary of findings 5 Glutamate modulators versus placebo for trichotillomania in adults; Summary of findings 6 Glutamate modulators versus placebo for trichotillomania in children and adolescents; Summary of findings 7 Opioid antagonists versus placebo for trichotillomania in adults; Summary of findings 8 SSRIs versus placebo for trichotillomania in adults; Summary of findings 9 TCAs with predominantly SRI actions versus placebo for trichotillomania in adults; Summary of findings 10 TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults

See summary of findings Table 1; summary of findings Table 2; summary of findings Table 3; summary of findings Table 4; summary of findings Table 5; summary of findings Table 6; summary of findings Table 7; summary of findings Table 8; summary of findings Table 9; summary of findings Table 10 for more information on the quality of the evidence.

Please refer to Types of outcome measures for a description of the scoring systems used in included studies.

Comparison 1: antioxidants versus placebo for trichotillomania in adults

Primary outcomes
Treatment response

The cross‐over study by Grant 2019 showed no evidence of benefit for silymarin (milk thistle extract) compared to placebo with regards to treatment response in adult participants after six weeks of treatment. On the Clinical Global Impressions ‐ Improvement scale (CGI‐I), 5 of 14 (35.7%) participants in the silymarin group compared to 4 of 14 (28.6%) participants in the placebo group showed "much" or "very much" improvement. This excludes data from four participants who were lost to follow‐up. There was no difference between groups when analysed using a best‐case scenario, ITT analysis (risk ratio (RR) 2.25, 95% confidence interval (CI) 0.84 to 5.99; 1 study, 36 participants; low‐certainty evidence; Analysis 1.1.1). We rated the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence interval.

Reduction of TTM symptom severity

In this single trial, adult participants in the silymarin group showed no difference in reduction of TTM symptom severity compared to those in the placebo group on any of the outcome scales employed, including the Clinical Global Impressions ‐ Severity scale (CGI‐S: mean difference (MD) ‐0.50, 95% CI ‐1.31 to 0.31; 1 study, 27 participants; low‐certainty evidence; Analysis 1.2.1), the Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS: MD ‐1.80, 95% CI ‐6.22 to 2.62; 1 study, 27 participants; low‐certainty evidence; Analysis 1.2.2), and the National Institute of Mental Health ‐ Trichotillomania Severity Scale (NIMH‐TSS: MD ‐1.00, 95% CI ‐5.00 to 3.00; 1 study, 27 participants; low‐certainty evidence; Analysis 1.2.3). We rated the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence intervals.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the adult participants of the Grant 2019 study, there was no evidence to support the treatment of comorbid symptoms of depression with silymarin versus placebo based on the HAM‐D scale (MD 0.60, 95% CI ‐1.82 to 3.02; 1 study, 27 participants; low‐certainty evidence; Analysis 1.3), and both groups were under the threshold for clinical depression at baseline and endpoint. We rated the certainty of this evidence as low for high imprecision due to small sample size and a wide confidence interval.

Quality of life ‐ functional disability

In the Grant 2019 study, quality of life in adults was assessed using the Sheehan Disability Scale (SDS). There was no evidence to support a beneficial effect of silymarin versus placebo for the improvement in functional impairment (MD ‐0.60, 95% CI ‐6.53 to 5.33; 1 study, 27 participants; low‐certainty evidence; Analysis 1.4). We rated the certainty of this evidence as low for high imprecision due to small sample size and a wide confidence interval.

Tolerability of treatment ‐ dropouts due to adverse events

In the Grant 2019 trial of silymarin versus placebo, no adult participants withdrew from the study as the result of adverse events (0% for silymarin versus 0% for placebo; 1 study, 18 participants; low‐certainty evidence; Analysis 1.5).

Tolerability of treatment ‐ common adverse events ( > 20%)

In the Grant 2019 trial, there were five reports of adverse events in the silymarin group; namely, nausea, upset stomach, bloating, insomnia and headache. In addition, there were four reports of nausea, upset stomach, bloating and dry mouth in the placebo group. The adverse effects were all of mild intensity. None of the adverse effects occurred at a rate of 20% or more. The trial did not report whether these were in adult or adolescent participants.

Comparison 2: antioxidants versus placebo for trichotillomania in adolescents

Primary outcomes
Treatment response

The adolescents in the study by Grant 2019 showed no difference between silymarin and placebo in terms of number of treatment responders using the CGI‐I scale, with two of four participants (50%) in the silymarin group showing response to treatment as compared to one of four (25%) in the placebo group, using an ITT analysis (RR 2.00, 95% CI 0.28 to 14.20; 1 study, 8 participants; low‐certainty evidence; Analysis 2.1). We rated the certainty of this evidence as low for high imprecision, due to small sample size and wide confidence interval.

Reduction of TTM symptom severity

Data calculated for adolescents in this trial showed no difference in reduction of TTM symptom severity for the silymarin group compared to those in the placebo group on any of the outcome scales employed, including the CGI‐S (MD ‐1.13, 95% CI ‐2.72 to 0.46; 1 study, 6 participants; low‐certainty evidence; Analysis 2.2.1), the MGH‐HPS (MD ‐5.87, 95% CI ‐17.46 to 5.72; 1 study, 6 participants; low‐certainty evidence; Analysis 2.2.2), the NIMH‐TSS (MD ‐2.94, 95% CI ‐8.14 to 2.26; 1 study, 6 participants; low‐certainty evidence; Analysis 2.2.3), the Trichotillomania Scale for Children ‐ Child version (TSC‐C: MD 0.00, 95% CI ‐1.25 to 1.25; 1 study, 6 participants; low‐certainty evidence; Analysis 2.2.4), and the TSC‐Parent version (TSC‐P: MD ‐1.20, 95% CI ‐1.48 to ‐0.92; 1 study, 6 participants; low‐certainty evidence; Analysis 2.2.5). We assessed the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence intervals.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the adolescents in the Grant 2019 study, there was no evidence to support the treatment of comorbid symptoms of depression with silymarin versus placebo using the HAM‐D scale (MD ‐1.62, 95% CI ‐3.98 to 0.74; 1 study, 7 participants; low‐certainty evidence; Analysis 2.3). Both the silymarin and placebo groups were under the threshold for clinical depression at baseline and endpoint. We rated the certainty of this evidence as low for high imprecision due to small sample size and a wide confidence interval.

Quality of life ‐ functional disability

Grant 2019 used the SDS to assess functional impairment for adolescents. There was no evidence to support a beneficial effect of silymarin versus placebo with regards to functional impairment (MD ‐1.30, 95% CI ‐8.43 to 5.83; 1 study, 6 participants; low‐certainty evidence; Analysis 2.4). We rated the certainty of this evidence as low for high imprecision due to small sample size and a wide confidence interval.

Tolerability of treatment ‐ dropouts due to adverse events

In the Grant 2019 trial of silymarin versus placebo, no adolescents withdrew from the study as the result of adverse events (0% for silymarin versus 0% for placebo; 1 study, 4 participants; low‐certainty evidence; Analysis 2.5).

Tolerability of treatment ‐ common adverse events ( > 20%)

As reported for adults above, in the single trial comparing silymarin to placebo, there were five reports of adverse effects in the silymarin group (nausea, upset stomach, bloating, insomnia and headache) and four reports of adverse effects in the placebo group (nausea, upset stomach, bloating and dry mouth), none of which occurred at a rate of 20% or more, and all of mild intensity. The trial did not report whether these were in adult or adolescent participants.

Comparison 3: antipsychotics versus placebo for trichotillomania in adults

Primary outcomes
Treatment response

The study by Van Ameringen 2010 yielded probable moderate treatment effects for olanzapine when compared with placebo on all primary outcome measures and was effective at a mean dose of 10.8 mg per day after a mean duration of 8.2 weeks (SD = 3.4 weeks).

On the CGI‐I in a single trial, those in the olanzapine group were more likely to respond to treatment compared with placebo, with 11 of 13 (85%) participants in the olanzapine group showing response to treatment compared to 2 of 12 (17%) in the placebo group, based on low‐certainty evidence (RR 5.08, 95% CI 1.40 to 18.37; 1 study, 25 participants; low‐certainty evidence; Analysis 3.1). The NNT with olanzapine to receive an additional beneficial outcome was 1.5 people (95% CI 1.0 to 2.5). We rated the certainty of the evidence as low due to high imprecision from a small sample size.

Reduction of TTM symptom severity

In a single trial, participants in the olanzapine group showed likely greater reduction in TTM symptom severity compared to those in the placebo group, as seen across all outcome scales employed, including the CGI‐S (MD ‐1.68, 95% CI ‐2.31 to ‐1.05; 1 study, 25 participants; low‐certainty evidence; Analysis 3.2.1), the MGH‐HPS (MD ‐4.87, 95% CI ‐8.84 to ‐0.90; 1 study, 25 participants; low‐certainty evidence; Analysis 3.2.2), and the Yale‐Brown Obsessive‐Compulsive Scale for Trichotillomania (TTM‐YBOCS) (MD ‐7.63, 95% CI ‐12.35 to ‐2.91; 1 study, 25 participants; low‐certainty evidence; Analysis 3.2.3). We rated the certainty of the evidence as low due to high imprecision from a small sample size. All effect sizes were moderate.

Secondary outcomes
Tolerability of treatment ‐ dropouts due to adverse events

In the Van Ameringen 2010 trial of olanzapine versus placebo, no participants withdrew from the study as the result of adverse effects (0% for olanzapine versus 0% for placebo; 1 study, 25 participants; low‐certainty evidence; Analysis 3.3).

Tolerability of treatment ‐ common adverse events ( > 20%)

In a single trial, the most common adverse effects in the olanzapine group compared to the placebo group were dry mouth (54% for olanzapine (N = 7) versus 0% for placebo; RR 13.93, 95% CI 0.88 to 220.37; 1 study, 25 participants; low‐certainty evidence; Analysis 3.4.1), fatigue (54% for olanzapine (N = 7) versus 0% for placebo; RR 13.93, 95% CI 0.88 to 220.37; 1 study, 25 participants; low‐certainty evidence; Analysis 3.4.2), increased appetite (46% for olanzapine (N = 6) versus 0% for placebo; RR 12.07, 95% CI 0.75 to 193.73; 1 study, 25 participants; low‐certainty evidence; Analysis 3.4.3), headache (38% for olanzapine (N = 5) versus 33% for placebo (N = 4); RR 10.21, 95% CI 0.62 to 167.12; 1 study, 25 participants; low‐certainty evidence; Analysis 3.4.4) and weight gain (38% for olanzapine (N = 5) versus 8% for placebo (N = 1); RR 10.21, 95% CI 0.62 to 167.12; 1 study, 25 participants; low‐certainty evidence; Analysis 3.4.5). Four of the 25 participants experienced no adverse events. We rated the certainty of this evidence as low due to high imprecision from a small sample size and wide confidence intervals.

Reduction of comorbid symptoms of depression

Treatment of comorbid symptoms of depression was an outcome of interest in the Van Ameringen 2010 study; however, no data were reported. A narrative summary reports little to no effect on the Beck Depression Inventory (Van Ameringen 2010). Summary statistics were not available for further analysis.

Quality of life ‐ functional disability

Quality of life was an outcome of interest in the Van Ameringen 2010 study; however, no data were reported. A narrative summary reports little to no effect on the SDS and on the Quality of Life Enjoyment and Satisfaction Questionnaire (Q‐LES‐Q) (Van Ameringen 2010. Summary statistics were not available for further analysis.

Comparison 4: cell signal transducers versus placebo for trichotillomania in adults

Primary outcomes
Treatment response

The study by Leppink 2017 showed no difference between inositol and placebo in terms of number of treatment responders using the CGI‐I scale with 8 of 19 (42.1%) in the inositol group showing response to treatment as compared to 6 of 12 (50%) in the placebo group, which excluded 7 participants who failed to complete the study. Using a best‐case scenario and ITT analysis, there was no effect of inositol on treatment response (RR 1.33, 95% CI 0.57 to 3.11; 1 study, 38 participants; low‐certainty evidence; Analysis 4.1). We judged the certainty of this evidence as low due to high imprecision, small sample size and wide confidence interval.

Reduction of TTM symptom severity

Using data from the trial protocol (NCT01875445 on ClinicalTrials.gov) we calculated the effect size of inositol versus placebo and found no difference between inositol and placebo in the reduction of TTM symptom severity on the MGH‐HPS (MD ‐1.30, 95% CI ‐5.12 to 2.52; 1 study, 38 participants; low‐certainty evidence; Analysis 4.2.1) or on the NIMH‐TSS (MD 0.00, 95% CI ‐3.37 to 3.37; 1 study, 38 participants; low‐certainty evidence; Analysis 4.2.2). We rated the certainty of this evidence as low due to high imprecision, small sample size and wide confidence intervals.

Secondary outcomes
Tolerability of treatment ‐ dropouts due to adverse events

In the Leppink 2017 trial of inositol versus placebo, no participants withdrew from the study as the result of adverse events (0% for inositol versus 0% for placebo; 1 study, 38 participants; low‐certainty evidence; Analysis 4.3).

Tolerability of treatment ‐ common adverse events ( > 20%)

In the Leppink 2017 study, within the inositol treatment group there were 11 minor adverse events reported and one case of ectopic pregnancy, a notable major adverse event. However, it was noted that the participant’s current birth control conferred an elevated risk of ectopic pregnancy, thus the event was likely unrelated to inositol.

Other minor adverse experiences reported were of mild intensity and included nausea or upset stomach (4 of 19 (21%) for inositol versus 2 of 19 (10.5%) for placebo; RR 2.00, 95% CI 0.41 to 9.65; 1 study, 38 participants; low‐certainty evidence; Analysis 4.4.1), stomach pain (10.5% for inositol versus 0% for placebo), diarrhoea (10.5% for inositol versus 0% for placebo), gas (5.3% for inositol versus 0% for placebo) and headache (10.5% for inositol versus 10.5% for placebo). RR was only calculated for adverse events with an incidence above 20%. There was little to no difference between groups regarding tolerability of treatment. We rated the certainty of this evidence as low due to high imprecision, small sample size and wide confidence interval.

Reduction of comorbid symptoms of depression

Leppink 2017 measured comorbid depressive symptoms using the Hamilton Depression Rating scale (HAM‐D) and found little to no treatment type‐by‐time interaction for inositol versus placebo (Leppink 2017). No further data were available for analysis.

Quality of life ‐ functional disability

Leppink 2017 measured quality of life using the Quality of Life Inventory (QoLI) and SDS, and found little to no treatment type‐by‐time interactions for inositol versus placebo. No further data were available for analysis (Leppink 2017).

Comparison 5: glutamate modulators versus placebo for trichotillomania in adults

Primary outcomes
Treatment response

The study by Grant 2009 of N‐acetylcysteine (NAC) versus placebo shows that NAC at a dose of 1200 mg twice a day was probably effective when compared with placebo. This finding was based on all primary outcome measures, although it is based on a single trial. NAC had a probable treatment effect on the CGI‐I compared to placebo, with a 3.5 times greater chance of responding to treatment for those receiving NAC (RR 3.50, 95% CI 1.34 to 9.17; 1 study, 50 participants; moderate‐certainty evidence; Analysis 5.1), and a number needed to treat (NNT) for an additional favourable outcome of 2.5 people (95% CI of 2 to 6). We judged the certainty of the evidence as moderate, downgrading for imprecision due to small sample size.

Reduction of TTM symptom severity

Reduction of symptoms as measured by the CGI‐S showed a probable benefit for NAC over placebo, although based on a single trial (MD ‐1.24, 95% CI ‐1.93 to ‐0.55; 1 study, 50 participants; moderate‐certainty evidence; Analysis 5.2.1). This likely beneficial effect in favour of NAC over placebo was also found on the patient‐rated MGH‐HPS (MD ‐5.60, 95% CI ‐8.50 to ‐2.70; 1 study, 50 participants; moderate‐certainty evidence; Analysis 5.2.2) and the Psychiatric Institute Trichotillomania Scale (PITS: MD ‐6.90, 95% CI ‐10.56 to ‐3.24; 1 study, 50 participants; moderate‐certainty evidence; Analysis 5.2.3). The treatment effect on the MGH‐HPS was first noted at nine weeks. We judged the certainty of the evidence as moderate for each scale, and downgraded for imprecision due to small sample size.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the Grant 2009 study, which compared NAC to placebo, depression severity was assessed using the HAM‐D. No clinical depression was detected in the group at baseline. No evidence was found to support the treatment of comorbid depression with NAC compared to placebo, based on a single trial (HAM‐D: MD ‐0.96, 95% CI ‐2.88 to 0.96; 1 study, 50 participants; low‐certainty evidence; Analysis 5.3). We judged the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence interval.

Quality of life ‐ functional disability

For NAC versus placebo, SDS was used to measure psychosocial functioning and quality of life. Although there appeared to be some improvement in functioning and quality of life for those assigned to the NAC group, the evidence suggests no difference for the outcome on the Sheehan Disability Scale, based on a single trial (SDS: MD ‐2.76, 95% CI ‐5.58 to 0.06; 1 study, 50 participants; low‐certainty evidence; Analysis 5.4) (Grant 2009). We rated the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence interval.

Tolerability of treatment ‐ dropouts due to adverse events

In the Grant 2009 trial of NAC versus placebo, no participants withdrew from the study as the result of adverse events (0% for NAC versus 0% for placebo; 1 study, 50 participants; low‐certainty evidence; Analysis 5.5).

Tolerability of treatment ‐ common adverse events ( > 20%)

In the Grant 2009 trial of NAC versus placebo, participants receiving NAC (N = 25) did not experience any adverse effects. Of participants receiving placebo (N = 25), one complained of nausea (4%), two of diarrhoea (8%) and one of cough (4%). We did not calculate the risk ratio as no adverse event had a prevalence higher than 20%.

Comparison 6: glutamate modulators versus placebo for trichotillomania in children and adolescents

Primary outcomes
Treatment response

The study by Bloch 2013 of N‐acetylcysteine (NAC) versus placebo showed little to no treatment effect on the CGI‐I for NAC, although based on a single trial in children and adolescents (RR 1.19, 95% CI 0.37 to 3.77; 1 study, 39 participants; Analysis 6.1). We rated the certainty of this evidence as low due to high imprecision from a small sample size and wide confidence interval.

Reduction of TTM symptom severity

Evidence for TTM symptom severity reduction, as measured by the MGH‐HPS, suggests a potentially large benefit for NAC over placebo in reducing TTM symptom severity, although based on a single trial in children and adolescents (MD ‐2.83, 95% CI ‐3.76 to ‐1.90; 1 study, 39 participants; low‐certainty evidence; Analysis 6.2.1). A likely effect in favour of NAC over placebo was also found on the NIMH‐TSS (MD ‐1.33, 95% CI ‐1.97 to ‐0.69; 1 study, 39 participants; low‐certainty evidence; Analysis 6.2.2). Little to no effect was found for NAC compared to placebo on the Trichotillomania Scale for Children ‐ Child version (TSC‐C: MD ‐0.08, 95% CI ‐0.22 to 0.06; 1 study, 39 participants; low‐certainty evidence; Analysis 6.2.3) or Parent version (TSC‐P: MD ‐0.05, 95% CI ‐0.16 to 0.06; 1 study, 39 participants; low‐certainty evidence; Analysis 6.2.4). We rated the certainty of this evidence as low due to high imprecision from a small sample size.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the Bloch 2013 study, which compared NAC to placebo, depression severity was assessed using the Children's Depression Inventory (CDI). At baseline assessment, 20% of participants reported current depression. The evidence suggests benefit for the placebo group compared to the NAC group on the CDI, although based on a single trial (MD 3.1, 95% CI 1.91 to 4.29; 1 study, 39 participants; low‐certainty evidence; Analysis 6.3). We rated the certainty of this evidence as low due to high imprecision from a small sample size.

Tolerability of treatment ‐ dropouts due to adverse events

In the Bloch 2013 trial of NAC versus placebo, one participant in the NAC group developed a whole‐body rash at week 4 and withdrew from the study as a result of this adverse event. There was no difference between NAC and placebo groups regarding attrition rate due to adverse events (5% for NAC versus 0% for placebo; RR 2.86, 95% CI 0.12 to 66.11; 1 study, 39 participants; low‐certainty evidence; Analysis 6.4). We rated the certainty of this evidence as low due to high imprecision from a small sample size and a wide confidence interval.

Tolerability of treatment ‐ common adverse events ( > 20%)

In the Bloch 2013 trial of NAC versus placebo, nausea was experienced by participants receiving both NAC (6 of 20; 30%) and placebo (12 of 19; 63%). Nausea was reported more frequently in the placebo group in this single trial (RR 0.47, 95% CI 0.22 to 1.01; 1 study, 39 participants; low‐certainty evidence; Analysis 6.5). There were no other common adverse events ( > 20%) in either group. We rated the certainty of this evidence as low due to high imprecision from a small sample size and a wide confidence interval.

Quality of life ‐ functional disability

This was not an outcome of interest in the Bloch 2013 study; therefore, no data were available.

Comparison 7: opioid antagonists versus placebo for trichotillomania in adults

Two studies compared naltrexone to placebo (Christenson 1994; Grant 2014). We report the results of the two studies together, although we could not fully synthesise the results. Most analyses were possible for only one of the two studies (Grant 2014), due to lack of available data from the other study (Christenson 1994). However, we did conduct meta‐analysis for the first outcome of treatment response.

Primary outcomes
Treatment response

The study by Grant 2014 reports little to no difference between naltrexone and placebo in terms of number of treatment responders on the CGI‐I with 9 of 25 (36%) of those in the naltrexone group showing “much” or “very much” improvement as compared to 9 of 26 (34.6%) of those in the placebo group. The study by Christenson 1994 was not published, and the study authors have not kept the raw data. They report that three (43%) of the participants receiving naltrexone as compared to zero (0%) in the placebo group experienced a greater than 50% reduction in TTM symptom severity as measured by the NIMH‐TSS. Meta‐analysis showed no beneficial treatment effect; however, the evidence is very uncertain about the effect of opioid antagonists on treatment response (RR 2.14, 95% CI 0.25 to 18.17; I² = 59%; 2 studies, 68 participants; very low‐certainty evidence; Analysis 7.1). We rated the certainty of this evidence as very low due to inconsistency and high imprecision from a small sample size and a wide confidence interval.

Reduction of TTM symptom severity

In the study by Grant 2014, on the CGI‐S, there was no effect of naltrexone versus placebo in reducing TTM symptom severity (MD ‐0.37, 95% CI ‐1.10 to 0.36; 1 study, 51 participants; low‐certainty evidence; Analysis 7.2.1). On the MGH‐HPS, their primary outcome for reduction in TTM symptom severity, there was no effect of naltrexone versus placebo (MD ‐1.14, 95% CI ‐4.18 to 1.90; 1 study, 51 participants; low‐certainty evidence; Analysis 7.2.2). Using the NIMH‐TSS scale, there was also no effect seen (MD ‐0.79, 95% CI ‐3.62 to 2.04; 1 study, 51 participants; low‐certainty evidence; Analysis 7.2.3). We rated the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence intervals.

Christenson 1994 reported evidence for benefit of naltrexone based on the NIMH‐TSS, although summary statistics were unavailable for meta‐analysis. The other outcome measures, however, did not yield evidence in favour of naltrexone on the NIMH‐Trichotillomania Impairment Scale (NIMH‐TIS), the NIMH Physician Rating Scale score, the number of hair‐pulling episodes, and the estimated number of hairs pulled as per narrative summaries in the original abstract. We did not assess the certainty of the evidence for this study as we were unable to calculate MD or SMD, and it was not clear which statistical tests were employed.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the Grant 2014 study, there was no evidence to support the treatment of comorbid symptoms of depression with naltrexone versus placebo based on the HAM‐D scale (MD 0.66, 95% CI ‐1.26 to 2.58; 1 study, 51 participants; low‐certainty evidence; Analysis 7.3), and both groups were under the threshold for clinical depression at baseline and endpoint. We rated the certainty of the evidence as low for high imprecision due to small sample size and a wide confidence interval.

In the Christenson 1994 study, no data measuring comorbid symptoms of depression were available as this was not an outcome of interest.

Quality of life ‐ functional disability

In the Grant 2014 study, no evidence was found on the SDS to support the use of naltrexone versus placebo for the reduction of functional disability (MD ‐1.91, 95% CI ‐5.82 to 2.00; 1 study, 51 participants; low‐certainty evidence; Analysis 7.4). We rated the certainty of the evidence as low due to high imprecision from a small sample size and a wide confidence interval.

Quality of life ‐ reduction of functional disability was not an outcome of interest for the other naltrexone trial (Christenson 1994); therefore, no data were available.

Tolerability of treatment ‐ common adverse events ( > 20%)

In the Grant 2014 study of naltrexone, there were few adverse experiences. Sedation was the only reported adverse effect that occurred more frequently in those taking naltrexone (3 of 25; 12%) compared to placebo (1 of 26; 3.8%), although based on a single trial (RR 3.12, 95% CI 0.35 to 28.03; 1 study, 51 participants; low‐certainty evidence; Analysis 7.5). Liver function testing by alanine aminotransferase (ALT), aspartate aminotransferase (AST) and ALT/AST ratio demonstrated little to no change between or within groups from baseline to endpoint. We rated the certainty of the evidence as low due to high imprecision from a small sample size and wide confidence interval.

No data related to adverse effects were derived from the other trial on naltrexone versus placebo as this was not an outcome of interest (Christenson 1994).

Tolerability of treatment ‐ dropouts due to adverse events

This was not an outcome of interest in either the Grant 2014 or Christenson 1994 studies; therefore, no data were available.

Comparison 8: SSRIs versus placebo for trichotillomania in adults

Within the SSRI class, two studies of fluoxetine versus placebo presented drug‐by‐period interaction data as F, df and P values (Christenson 1991a; Streichenwein 1995). Neither of the principal authors of these studies was able to provide the original data from the trials to make individual participant analysis (IDP) possible. Therefore, we describe the results of these trials individually. For the third SSRI study, a sertraline study, we obtained mean change scores for the primary outcome measure from the first author (Dougherty 2006). None of the SSRI trials reported effect of SSRI on treatment response compared to placebo; therefore, data were unavailable for further analysis of this outcome.

Primary outcomes
Treatment response

Dichotomous treatment response was not an outcome of interest in the Christenson 1991a, Dougherty 2006 or Streichenwein 1995 studies; therefore, no further data were available for analysis.

Reduction of TTM symptom severity

Results of the initial 12‐week phase of the Dougherty 2006 trial comparing sertraline versus placebo were not published, as this phase of the trial was not the focus of the study. We obtained from the first author the mean change scores on their primary outcome measure, the MGH‐HPS (mean change score for sertraline = ‐1.53, SD 5.54; mean change score for placebo = ‐1.06, SD 5.34). Our analysis showed the evidence was very uncertain with regards to the effect of sertraline compared with placebo in reduction of TTM symptom severity, based on a single trial (MD ‐0.47, 95% CI ‐4.30 to 3.36; 1 study, 31 participants; very low‐certainty evidence; Analysis 8.2). We judged the certainty of this evidence as very low due to indirectness (using mean change scores rather than MD), high imprecision (wide confidence interval and small sample size) and risk of attrition bias.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the cross‐over study by Christenson 1991a, mean baseline scores on both the HAM‐D and the BDI were below the threshold for clinical depression. Mean differences between fluoxetine and placebo showed no difference on either scale (HAM‐D: MD 0.80, 95% CI ‐1.90 to 3.50; 1 study, 32 participants; low‐certainty evidence; Analysis 8.3). A drug‐by‐period interaction was noted for the HAM‐D scores, but in the opposite direction of that anticipated: an improvement in depression was observed during the placebo phase and a worsening of depression during the fluoxetine phase. We rated the certainty of this evidence as low due to imprecision with a wide confidence interval and small sample size.

In the cross‐over study by Streichenwein 1995, mean baseline scores on both the HAM‐D and the BDI were below the threshold for clinical depression. Scores from the fluoxetine and placebo treatment periods were combined, so that the effect of fluoxetine cannot be differentiated from the effect of placebo. No drug‐by‐period interaction was reported for the HAM‐D or the BDI. We did not rate the certainty of this evidence as we were unable to calculate MD or SMD.

No data were available on symptoms of comorbid depression for the pharmacotherapy phase of the trial comparing sertraline versus placebo (Dougherty 2006). However, a narrative summary stated that there were no differences between groups observed on final scores on the HAM‐D or BDI (Dougherty 2006).

Tolerability of treatment ‐ dropouts due to adverse events

In the Christenson 1991a cross‐over trial of fluoxetine versus placebo, 1 of 17 participants (5.9%) withdrew from the trial after developing urticaria during week four of fluoxetine. In the Streichenwein 1995 cross‐over trial of fluoxetine versus placebo, 1 of 23 participants (4.3%) withdrew from the trial during the fluoxetine phase because of a severe serum sickness–like syndrome during week seven. Meta‐analysis shows no effect of fluoxetine on dropouts due to adverse events, based on two trials (5.1% for SSRI versus 0% for placebo; RR 3.00, 95% CI 0.33 to 27.62; I² = 0%; 2 studies, 78 participants; low‐certainty evidence; Analysis 8.4). We judged the certainty of this evidence as low due to high imprecision from a small sample size and wide confidence interval. No data were available on adverse drug effects for the pharmacotherapy phase of the trial comparing sertraline to placebo, as it was not an outcome of interest for this study (Dougherty 2006).

Tolerability of treatment ‐ common adverse events ( > 20%)

In the Christenson 1991a trial, the most common adverse event was nausea, which was reported in 5 of 17 (29.4%) participants taking fluoxetine and in 2 of 17 (11.8%) of participants taking placebo (RR 2.5, 95% CI 0.56 to 11.16; 1 study, 34 participants; low‐certainty evidence; Analysis 8.5.1). We rated the certainty of this evidence as low due to high imprecision and risk of attrition bias. In the Streichenwein 1995 trial, common adverse events were categorised as central nervous system (CNS) and gastrointestinal (GIT) effects. CNS effects (including nightmares, insomnia, dizziness, irritability, anxiety and a feeling of doom) as a category affected 22 of 23 participants (95.7%) during the fluoxetine phase of the trial versus 16 of 23 participants (69.6%) during the placebo phase in this single trial (RR 1.38, 95% CI 1.04 to 1.83; 1 study, 46 participants; low‐certainty evidence; Analysis 8.5.2). GIT effects (including decreased appetite, diarrhoea, constipation, nausea, increased weight, abdominal pain and dyspepsia) as a category affected 14 of 23 participants (60.9%) in the fluoxetine phase of the trial and only 3 of 23 participants (13.0%) during the placebo phase (RR 4.67, 95% CI 1.55 to 14.09; 1 study, 46 participants; low‐certainty evidence; Analysis 8.5.3). We rated the certainty of this evidence as low due to high imprecision and risk of attrition bias. No data were available on adverse drug effects for the pharmacotherapy phase of the trial comparing sertraline versus placebo as it was not an outcome of interest for this trial (Dougherty 2006).

Quality of life ‐ functional disability

There were no data available for analysis of the effect of sertraline on quality of life or functional disability compared to placebo. A narrative summary of the effect of sertraline on quality of life compared to placebo states that no differences between groups were observed in final scores on the Quality of Life Enjoyment and Satisfaction Questionnaire (Q‐LES‐Q) (Dougherty 2006).

Data were unavailable from the fluoxetine versus placebo trials as quality of life was not an outcome of interest in these studies (Christenson 1991a; Streichenwein 1995).

Comparison 9: TCAs with predominantly SRI actions versus placebo for trichotillomania in adults

One parallel‐arm trial of clomipramine versus placebo is included in the review (Ninan 2000). The evidence was very uncertain regarding the efficacy of clomipramine in this study.

Primary outcomes
Treatment response

In the study by Ninan 2000, scores on the CGI‐I favoured clomipramine, with 4 of 10 participants in the clomipramine group showing response to treatment, compared with 0 of 6 in the placebo group. The evidence from this single trial was very uncertain (RR 5.73, 95% CI 0.36 to 90.83; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.1). We rated the overall certainty of the evidence as very low due to risk of attrition bias and high imprecision from a small sample size and wide confidence interval.

Reduction of TTM symptom severity

Reduction of TTM symptom severity was reported on the NIMH‐TIS and the NIMH‐TSS. On the NIMH‐TIS, there was very uncertain evidence about the effect of clomipramine on the reduction of TTM symptom severity compared to placebo, based on a single trial (MD 1.60, 95% CI ‐0.82 to 4.02; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.2.1). We rated the certainty of the evidence as very low due to risk of attrition bias and high imprecision due to small sample size and wide confidence interval.

On the NIMH‐TSS, there was very uncertain evidence about the effect of clomipramine on the reduction of TTM symptom severity compared to placebo in a single trial (MD ‐3.00, 95% CI ‐6.52 to 0.52; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.2.2). We rated the certainty of the evidence as very low due to risk of attrition bias and high imprecision due to small sample size and wide confidence interval.

Secondary outcomes
Tolerability of treatment ‐ dropouts due to adverse events

In the Ninan 2000 trial of clomipramine versus placebo, 3 of 10 participants (30%) receiving clomipramine dropped out of the study because of significant drug‐related adverse effects, although it is not stated which adverse effects caused participants to withdraw from the study. There was very uncertain evidence for increased dropouts due to adverse events in the clomipramine group compared to the placebo group, based on this single trial (30% for clomipramine versus 0% for placebo; RR 4.45, 95% CI 0.27 to 73.81; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.3). We rated the certainty of the evidence as very low due to risk of attrition bias and high imprecision from a small sample size and wide confidence interval.

Tolerability of treatment ‐ common adverse events ( > 20%)

Common adverse effects in participants taking clomipramine, in a single trial, were tremor (3 of 10; 30%) (RR 4.45, 95% CI 0.27 to 73.81; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.4.1), sedation (2 of 10; 20%) (RR 3.18, 95% CI 0.18 to 56.95; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.4.2), dry mouth (2 of 10; 20%) (RR 3.18, 95% CI 0.18 to 56.95; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.4.3) and constipation (2 of 10; 20%) (RR 3.18, 95% CI 0.18 to 56.95; 1 study, 16 participants; very low‐certainty evidence; Analysis 9.4.4). There is very uncertain evidence regarding the effect of clomipramine compared to placebo on the risk of experiencing the above adverse events, although the six participants who were taking placebo in the Ninan 2000 trial reported no adverse events. We rated the certainty of this evidence as very low due to high imprecision from small sample size, wide confidence intervals and risk of attrition bias.

Reduction of comorbid symptoms of depression

This was not an outcome of interest in the Ninan 2000 study; therefore, no further data were available for analysis.

Quality of life ‐ functional disability

This was not an outcome of interest in the Ninan 2000 study; therefore, no further data were available for analysis.

Comparison 10: TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults

Primary outcomes
Treatment response

The Swedo 1989 study provided evidence that clomipramine may be effective when compared with desipramine on the unvalidated Physician‐Rated Clinical Progress scale (PRCP) for treatment response (MD ‐4.00, 95% CI ‐6.13 to ‐1.87; 1 study, 26 participants; low‐certainty evidence; Analysis 10.1). We rated the certainty of the evidence as low due to high imprecision from a small sample size. Dichotomous treatment response was not measured using a formal scale in the original study, and therefore dichotomous treatment response is not available for analysis.

Reduction of TTM symptom severity

Clomipramine may have a beneficial effect on the reduction of TTM symptom severity compared to desipramine on the NIMH‐TIS, although based on a single trial (MD ‐2.00, 95% CI ‐3.58 to ‐0.42; 1 study, 26 participants; low‐certainty evidence; Analysis 10.2.1). On another measure, the NIMH‐TSS, in the same trial clomipramine showed no effect on reduction of TTM symptom severity (MD ‐3.80, 95% CI ‐8.08 to 0.48; 1 study, 26 participants; low‐certainty evidence; Analysis 10.2.2). We assessed the overall certainty of this evidence as low due to high imprecision from a small sample size.

Secondary outcomes
Reduction of comorbid symptoms of depression

In the study by Swedo 1989, the NIMH‐GASD was used to assess severity of depression symptoms. The study authors report that no participants scored in the range of clinical depression at the beginning of the study. There was no difference in effect between clomipramine and desipramine (MD ‐0.7, 95% CI ‐1.6 to 0.2; 1 study, 26 participants; low‐certainty evidence; Analysis 10.3). We judged the overall certainty of this evidence as low due to high imprecision from a small sample size.

Tolerability of treatment ‐ dropouts due to adverse events

In the Swedo 1989 cross‐over study comparing clomipramine versus desipramine, of the 13 participants, none withdrew because of adverse events (0% for clomipramine versus 0% for desipramine; 1 study, 26 participants; low‐certainty evidence; Analysis 10.4).

Tolerability of treatment ‐ common adverse events ( > 20%)

The three common adverse events affecting participants in this single trial (N = 13) were constipation (5 of 13 (38.5%) for clomipramine compared with 6 of 13 (46.2%) for desipramine; RR 0.83, 95% CI 0.34 to 2.06; 1 study, 26 participants; low‐certainty evidence; Analysis 10.5.1), dry mouth (5 of 13 (38.5%) for clomipramine and 8 of 13 (61.5%) for desipramine; RR 0.63, 95% CI 0.28 to 1.41; 1 study, 26 participants; low‐certainty evidence; Analysis 10.5.2) and tremor (7 of 13 (53.8%) for clomipramine and 3 of 13 (23.1%) for desipramine; RR 2.33, 95% CI 0.77 to 7.10; 1 study, 26 participants; low‐certainty evidence; Analysis 10.5.3). The authors report that there were no differences between clomipramine and desipramine with regards to adverse effects. We judged the certainty of the evidence for common adverse events as low due to high imprecision from a small sample size and wide confidence intervals.

Quality of life ‐ functional disability

This was not an outcome of interest in the Swedo 1989 study; therefore, no further data were available for analysis.

Heterogeneity

There were not enough studies to permit investigation of heterogeneity and its clinical sources. Heterogeneity for individual outcomes is addressed in the relevant section above.

Subgroup analyses

There were insufficient studies to permit a subgroup analysis ( < 10 studies per subgroup).

Sensitivity analyses

There were insufficient studies to allow a sensitivity analysis ( < 10 studies for any single outcome).

Publication bias

There were insufficient studies to permit detection of publication bias ( < 10 studies in any comparison).

Discussion

Summary of main results

Overall, a small body of evidence is available on pharmacotherapy for TTM. Twelve studies, all RCTs, are included in this review, all published between 1989 and 2019. Three studies of SSRIs (Christenson 1991a; Dougherty 2006; Streichenwein 1995), two studies of TCAs with predominantly SRI actions (Ninan 2000; Swedo 1989), two studies of opioid antagonists (Christenson 1994; Grant 2014), and two studies of glutamate modulators were included (Bloch 2013; Grant 2009). The three remaining studies focused on an atypical antipsychotic (Van Ameringen 2010), an antioxidant (Grant 2019), and a cell signal transducer (Leppink 2017). The eleven studies in adults involved a total of 298 participants with a mean sample size of 27 participants per trial and a range of 13 (Swedo 1989), to 51 participants (Grant 2014). Only one included study was conducted exclusively in children and adolescents, which had a sample size of 39 participants (Bloch 2013). One study included 4 adolescent and 18 adult participants in a single cross‐over study (Grant 2019).

We did not conduct meta‐analysis across medication classes due to the varying neurochemical actions of the agents utilised. For adults, meta‐analysis within medication class was undertaken for the following select outcomes with sufficient data: treatment response to opioid antagonists across two studies (Christenson 1994; Grant 2014), and dropout rate due to adverse events with SSRIs across two studies (Christenson 1991a; Streichenwein 1995). The remaining classes each contained a single study (antioxidants, antipsychotics, cell signal transducers and glutamate modulators) or had multiple studies that could not be combined due to different comparator groups (TCAs with predominantly SRI actions). We primarily conducted analyses on data from single studies, generating summary statistics in the form of MDs and RRs for our outcomes of interest. For children and adolescents, we included only two studies in this review (Bloch 2013; Grant 2019). As they investigated different medications, meta‐analysis was not possible. For these studies of a glutamate modulator and an antioxidant, we report summary statistics in the form of MDs and RRs for our outcomes of interest.

Overall, it is difficult to draw high‐quality conclusions of treatment efficacy, as most medications are represented by a single, relatively small trial. However, four individual trials in adults demonstrated preliminary evidence for the possible efficacy of three individual agents. Clomipramine (a TCA with predominantly SRI action) showed potential benefit compared to desipramine in reducing TTM symptom severity, with low‐certainty (Swedo 1989). Olanzapine, an atypical antipsychotic, also showed a possible beneficial effect on treatment response compared to placebo, and reduced TTM symptom severity, again albeit with low‐certainty (Van Ameringen 2010). There was also evidence of a probable, beneficial effect of NAC (a glutamate modulator) on treatment response and reduction of TTM symptom severity in adults, with moderate‐certainty in the effect estimate, although based on a single trial (Grant 2009).

A single RCT in children and adolescents found evidence that NAC may have a potential beneficial effect on TTM symptom severity in children and adolescents compared to placebo (Bloch 2013). However, this finding may have been influenced by baseline differences between intervention and placebo groups on the MGH‐HPS and NIMH‐TSS. This finding was also not consistent across all rating scales of TTM symptom severity, suggesting the need for further studies, and certainty in this estimate is low. Moreover, the study showed no beneficial treatment effect of NAC when measuring treatment response on the CGI‐I (Bloch 2013). This may indicate differences in the neurobiology of TTM in adults and children. Additionally, the inconsistency between self‐reported and clinician‐rated scales suggests a need for further scale validation studies in children and adolescents with TTM. As trichotillomania is a disorder commonly occurring in childhood, this warrants further investigation.

The overall certainty of the evidence as per GRADE ratings was low on average, with only NAC having some moderate‐certainty evidence for possible beneficial effects in adults. Common factors for downgrading the certainty of evidence included wide confidence intervals and small sample size. We found no further substantial evidence of beneficial or harmful effects for fluoxetine, sertraline, desipramine, naltrexone, silymarin or inositol.

Overall completeness and applicability of evidence

We have presented data from all published and unpublished trials that assessed the efficacy and tolerability of pharmacotherapeutic options for adult TTM and TTM in children and adolescents. The current evidence base of RCTs is not sufficient to permit robust meta‐analysis; thus, there was insufficient evidence to confirm or refute the efficacy or acceptability of any particular agent or class of medication for the treatment of TTM in adults or in children and adolescents. There is a particular lack of randomised, placebo‐controlled trials for the treatment of paediatric TTM. As TTM often has its onset in childhood or adolescence, this is an important area that warrants further investigation.

The 12 included studies cover 7 different medication classes; therefore, evidence within individual medication classes is insufficient to generalise from individual agents to class. A greater number of larger studies across a broad range of medication classes is needed before robust conclusions can be drawn from meta‐analysis. Nevertheless, evidence from single studies suggests that certain medications (clomipramine, olanzapine, NAC) may provide some benefit in adults (Grant 2009; Swedo 1989; Van Ameringen 2010) or children and adolescents (NAC: Bloch 2013).

Meta‐analysis was restricted by methodological heterogeneity in terms of statistical reporting, and the use of a wide variety of TTM symptom scales, including some that have not been well validated or previously published. This is a matter of concern because evidence indicates that unpublished rating scales are more likely to favour the treatment group over the control group (Marshall 2000). Several possible reasons have been proposed for this, one of which is that post hoc 'adjustment' of unpublished scales by removing unfavourable items can skew the results in favour of the treatment group (Marshall 2000). In future studies, the use of one or two validated symptom scales, such as the CGI‐I and MGH‐HPS, and reporting group means and variance will enhance the meta‐analytic options.

It is important for future studies to include participants with psychiatric comorbidities, and to measure and report participant response to medication (e.g. depression and anxiety). The exclusion of participants with comorbid disorders means that study participants are likely not a good representation of clinical populations. Amongst the included studies in this review, three studies excluded participants with comorbid psychiatric disorders (Dougherty 2006; Swedo 1989; Van Ameringen 2010); three studies excluded participants with bipolar disorder, dementia, psychotic disorders or substance use disorders (Grant 2014; Grant 2019; Leppink 2017); one study excluded only participants with bipolar disorder or psychotic disorders (Grant 2009); and two studies did not specify comorbidities (Christenson 1994; Ninan 2000). The study exclusively in children and adolescents excluded participants with bipolar disorder, psychotic disorder, substance use disorder, developmental disorder or mental retardation (Bloch 2013). Where information about comorbidities was available, we extracted and reported it.

With the exception of clomipramine and desipramine, direct comparisons of the relative clinical effectiveness of medications in treating TTM are lacking. Direct comparisons of agents may shed light on the neurobiology and treatment of TTM. Clomipramine, which exhibits potent serotonergic activity, showed potential, positive treatment effects, which were lacking for other strongly serotonergic agents – namely, the SSRIs included in this study. This observation may be explained by clomipramine’s noradrenergic metabolite, desmethylclomipramine (Maj 1982). However, desipramine, which has strong noradrenergic effects, failed to produce potentially positive treatment effects. This suggests the involvement of both serotonergic and noradrenergic pathways and is supported by positive findings from an open‐label trial of venlafaxine, a serotonin‐noradrenaline reuptake inhibitor (SNRI), which has both serotonergic and noradrenergic effects (Ninan 1998). Thus, the role of specific monoamines requires further study with head‐to‐head comparisons of agents from within medication classes to investigate the roles of each neurotransmitter in turn.

A multiple‐treatment meta‐analysis (MTM) might be a useful method in future updates of this review to allow comparison of three or more different interventions (potentially from different studies) in one meta‐analysis. For MTM to be performed, the included studies would have to be similar in all ways other than the interventions being compared, which is currently not the case.

Given the relative lack of evidence to confirm or refute efficacy of any particular medication in treating TTM in adults or children and adolescents, the presence of a comorbid disorder that is known to be responsive to medication may be useful in choosing a medication. Currently, there is no established first‐line recommendation for medication in TTM (Farhat 2020; Grant 2016). The presence of psychiatric comorbidities, such as anxiety or depressive disorders, may play a role in selecting an appropriate treatment option. Similarly, knowledge of common adverse events associated with each medication may further assist clinical decision‐making.

Whilst medication may provide some benefit in treating TTM, habit‐reversal therapy and other psychotherapeutic approaches remain viable first‐line treatment options, as discussed in other reviews (Bloch 2007; Farhat 2020; Rehm 2015).

Future treatment options include the cannabinoid agonist dronabinol (NCT03530800 on ClinicalTrials.gov; NCT03530800), an experimental drug targeting System xc‐ called SXC‐2023 (NCT03797521 on ClinicalTrials.gov; NCT03797521), and other NAC derivatives that improve blood‐brain barrier permeability being developed by Promentis Pharmaceuticals (patents.google.com/patent/WO2015070034A1/en).

Quality of the evidence

This review included 12 studies of 341 participants, in total spanning 7 different medication classes (SSRIs, TCAs, antipsychotics, opioid antagonists, glutamate modulators, antioxidants and cell signal transducers). The number of participants in the included studies was very small, ranging from 13 to 51, and 4 of the 12 included studies had fewer than 20 participants. Small sample size was the primary reason for downgrading the certainty of the evidence.

In addition to these small numbers, attrition rates of greater than 10% were seen in 7 of the 12 trials (Bloch 2013; Dougherty 2006; Grant 2014; Grant 2019; Leppink 2017; Ninan 2000; Streichenwein 1995). In the Dougherty 2006 study, 37 participants were randomly assigned, but only 31 of the 37 participants had their outcome data included in the final analysis, representing an attrition rate of 19%. In the Ninan 2000 study, 23 participants were randomly assigned and data from only 16 participants were analysed, for an attrition rate of 30%. In the Streichenwein 1995 study, 23 participants were randomly assigned with data from only 16 participants included in the final analysis, for an attrition rate of 30%. These trials did not employ intention‐to‐treat (ITT) analyses, representing a high risk of attrition bias. Four other studies by Bloch 2013, Grant 2014, Grant 2019 and Leppink 2017 had attrition rates of 10% (4 of 39 participants), 14% (7 of 51 participants), 18% (4 of 22 participants) and 18% (7 of 38 participants), respectively, but all randomised participants were included in analyses using an ITT principle.

The use of different, unvalidated scales in some of the included studies diminishes the certainty of evidence available from these studies. For example, two studies used a self‐reported rating scale that relied on participants to count the number of hair‐pulling episodes, as well as to rate the urgency and severity of hair‐pulling (Christenson 1991a; Streichenwein 1995). Given that hair‐pulling is often done without awareness, participants may be limited in their ability to keep track of their own hair‐pulling.

Protocols for some of these trials were not publicly available, which limited our ability to determine whether there was reporting bias that might in turn have influenced outcomes. In line with other efforts to enhance replicability, we would encourage publication of TTM clinical trial protocols in the future. More recent trials had published protocols on the ClinicalTrials.gov portal (www.clinicaltrials.gov/), which aids interrogation of possible reporting bias.

Four of the trials included in this review employed a cross‐over design (Christenson 1991a; Grant 2019; Streichenwein 1995; Swedo 1989). Failure to include a washout period in the Swedo 1989 trial comparing clomipramine with desipramine may have impacted the trial results because of the persistent effects of these agents on both TTM and comorbid conditions such as depression.

The limited number of studies and the limited number of participants, as well as the high attrition rates in many of the studies and the lack of intention‐to‐treat analyses, indicate that any conclusions about the use of medication for treating TTM must be made with caution. The NAC and olanzapine trials in adults are methodologically robust (Grant 2009; Van Ameringen 2010). However, the certainty of the evidence (GRADE) from a meta‐analytic perspective for treatment response and reduction of TTM symptom severity was moderate for NAC and low for olanzapine (downgraded for high imprecision from small sample sizes). Moderate‐certainty evidence implies that further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate, whereas low‐certainty evidence implies that further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. These studies deserve replication to further examine the efficacy of olanzapine and NAC for TTM in adults.

Over time, we note more consistent reporting of outcomes in both published articles on TTM and protocols on ClinicalTrials.gov. In addition, there have been improvements in study design, use of validated scales and reduction of risk of bias in the included studies, with newer studies reporting outcomes as intention‐to‐treat analyses. More high‐quality trials that are appropriately powered are required before a robust meta‐analysis can be undertaken. Psychometric evaluation of validated, clinician‐rated scales would also aid future synthesis of findings.

Potential biases in the review process

We attempted to be as comprehensive as possible in the review process. As recommended for all Cochrane reviews, we conducted an extensive and comprehensive search of multiple electronic bibliographic databases to identify trials eligible for inclusion. We applied no language or publication restrictions in our search. Further, we engaged directly with many of the authors to obtain missing data or to ask for clarification when this was required. We minimised potential bias in the conduct of our review by having two independent researchers extract data and assess the methodological quality of each study. This detailed process allowed a thorough assessment of trial conduct and an exploration of the possible biases that may be present in each trial. Despite all of the measures taken, it is possible that unpublished data have been reported that we did not find; this represents a potential bias in the review process.

Agreements and disagreements with other studies or reviews

The methodology employed in this study differs from that employed in the meta‐analysis of pharmacological trials conducted by Bloch 2007, Farhat 2020 and McGuire 2014. Unlike in the present review, Bloch 2007, Farhat 2020 and McGuire 2014 chose to perform a meta‐analysis of the SSRI trials (Christenson 1991a; Dougherty 2006; Streichenwein 1995), and included a fourth trial, Van Minnen 2003, which the present review excluded in view of its waiting‐list control group (i.e. lack of a placebo group). In addition, Bloch 2007 and Farhat 2020 included trials that used different rating scales. The review authors did not find a statistically significant benefit of SSRIs over placebo (Bloch 2007; Farhat 2020). In the meta‐analysis of the clomipramine trials, Bloch 2007 and Farhat 2020 found that clomipramine demonstrated efficacy compared with placebo or active control conditions, and this difference was found to be statistically significant. In the present review, we decided that it was not appropriate to combine the two clomipramine trials in a meta‐analysis, as one used a placebo group as a control and the other used desipramine as a control (Ninan 2000; Swedo 1989). McGuire 2014 combined SSRIs and TCAs with predominantly SRI actions in a meta‐analysis and found a significant treatment effect (SMD 0.41). We chose not to combine these classes in a meta‐analysis due to heterogeneity in neurochemical actions. Finally, we report treatment response in terms of a dichotomised measure of the CGI‐I, which is not reported on by Bloch 2007, Farhat 2020 or McGuire 2014.

Compared to our original review, we have included summary of findings tables, applied GRADE criteria to rate the certainty in the evidence presented, included three new studies in adults (Grant 2014; Grant 2019; Leppink 2017), and included two new studies in children and adolescents (Bloch 2013; Grant 2019). Additionally, we calculated the number needed to treat for an additional beneficial outcome (NNTB) for NAC and olanzapine in adults. We also include additional graphs and analyses for all outcomes, including meta‐analyses for select outcomes within medication classes and for total effectiveness of medication in TTM.

PRISMA flow diagram

Figures and Tables -
Figure 1

PRISMA flow diagram

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies

Figures and Tables -
Figure 2

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies

Risk of bias summary: review authors' judgements about each risk of bias item for each included study

Figures and Tables -
Figure 3

Risk of bias summary: review authors' judgements about each risk of bias item for each included study

Comparison 1: Antioxidants versus placebo in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 1.1

Comparison 1: Antioxidants versus placebo in adults, Outcome 1: Treatment response

Comparison 1: Antioxidants versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 1.2

Comparison 1: Antioxidants versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 1: Antioxidants versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 1.3

Comparison 1: Antioxidants versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 1: Antioxidants versus placebo in adults, Outcome 4: Quality of Life ‐ functional disability

Figures and Tables -
Analysis 1.4

Comparison 1: Antioxidants versus placebo in adults, Outcome 4: Quality of Life ‐ functional disability

Comparison 1: Antioxidants versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 1.5

Comparison 1: Antioxidants versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 1: Treatment response

Figures and Tables -
Analysis 2.1

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 1: Treatment response

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 2.2

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 2: Reduction of TTM symptom severity

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 2.3

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 4: Quality of Life ‐ functional disability

Figures and Tables -
Analysis 2.4

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 4: Quality of Life ‐ functional disability

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 5: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 2.5

Comparison 2: Antioxidants versus placebo in adolescents, Outcome 5: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 3: Antipsychotics versus placebo in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 3.1

Comparison 3: Antipsychotics versus placebo in adults, Outcome 1: Treatment response

Comparison 3: Antipsychotics versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 3.2

Comparison 3: Antipsychotics versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 3: Antipsychotics versus placebo in adults, Outcome 3: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 3.3

Comparison 3: Antipsychotics versus placebo in adults, Outcome 3: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 3: Antipsychotics versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 3.4

Comparison 3: Antipsychotics versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Common adverse events (> 20%)

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 4.1

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 1: Treatment response

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 4.2

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 3: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 4.3

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 3: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 4.4

Comparison 4: Cell signal transducers versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Common adverse events (> 20%)

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 5.1

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 1: Treatment response

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 5.2

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 5.3

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 4: Quality of Life ‐ functional disability

Figures and Tables -
Analysis 5.4

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 4: Quality of Life ‐ functional disability

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 5.5

Comparison 5: Glutamate modulators versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 1: Treatment response

Figures and Tables -
Analysis 6.1

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 1: Treatment response

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 6.2

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 2: Reduction of TTM symptom severity

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 6.3

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 4: Tolerability of treatment ‐ Dropouts due to adverse eventsDropouts due to adverse events

Figures and Tables -
Analysis 6.4

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 4: Tolerability of treatment ‐ Dropouts due to adverse eventsDropouts due to adverse events

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 6.5

Comparison 6: Glutamate modulators versus placebo in children and adolescents, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 7.1

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 1: Treatment response

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 7.2

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 7.3

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 4: Quality of Life ‐ functional disability

Figures and Tables -
Analysis 7.4

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 4: Quality of Life ‐ functional disability

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 7.5

Comparison 7: Opioid antagonists versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Treatment response

Study

Heading 1

Figures and Tables -
Analysis 8.1

Comparison 8: SSRIs versus placebo in adults, Outcome 1: Treatment response

Comparison 8: SSRIs versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 8.2

Comparison 8: SSRIs versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 8: SSRIs versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 8.3

Comparison 8: SSRIs versus placebo in adults, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 8: SSRIs versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 8.4

Comparison 8: SSRIs versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 8: SSRIs versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 8.5

Comparison 8: SSRIs versus placebo in adults, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 9.1

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 1: Treatment response

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 9.2

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 3: Tolerability of treatment ‐ Dropouts due to adverse eventsDropouts due to adverse events

Figures and Tables -
Analysis 9.3

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 3: Tolerability of treatment ‐ Dropouts due to adverse eventsDropouts due to adverse events

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 9.4

Comparison 9: TCAs with predominantly SRI actions versus placebo in adults, Outcome 4: Tolerability of treatment ‐ Common adverse events (> 20%)

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 1: Treatment response

Figures and Tables -
Analysis 10.1

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 1: Treatment response

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 2: Reduction of TTM symptom severity

Figures and Tables -
Analysis 10.2

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 2: Reduction of TTM symptom severity

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 3: Reduction of comorbid symptoms of depression

Figures and Tables -
Analysis 10.3

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 3: Reduction of comorbid symptoms of depression

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 4: Tolerability of treatment ‐ Dropouts due to adverse events

Figures and Tables -
Analysis 10.4

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 4: Tolerability of treatment ‐ Dropouts due to adverse events

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Figures and Tables -
Analysis 10.5

Comparison 10: TCAs with predominantly SRI actions versus other TCAs in adults, Outcome 5: Tolerability of treatment ‐ Common adverse events (> 20%)

Summary of findings 1. Antioxidants versus placebo for trichotillomania in adults

Antioxidants versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: antioxidants versus placebo in adults

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Antioxidants versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) or similar (no. of responders)

Follow‐up: 6 weeks

Study population

RR 2.25
(0.84 to 5.99)

36
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the antioxidant group and the placebo group in adults.

222 per 1000

500 per 1000
(187 to 1000)

Moderate

222 per 1000

500 per 1000
(186 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 6 weeks

The mean MGH‐HPS score for the antipsychotic intervention group was 12.5.

The mean reduction of TTM symptom severity in the intervention groups was 1.8 lower
(6.22 lower to 2.62 higher).

27
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the antioxidant group compared to the placebo group on the MGH‐HPS in adults.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate

Follow‐up: 6 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

18
(1 study)

⊕⊕⊝⊝
lowb

The evidence is uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).

Figures and Tables -
Summary of findings 1. Antioxidants versus placebo for trichotillomania in adults
Summary of findings 2. Antioxidants versus placebo for trichotillomania in adolescents

Antioxidants versus placebo for trichotillomania in adolescents

Patient or population: children with trichotillomania
Settings: outpatient
Intervention: antioxidants versus placebo in adolescents

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Antioxidants versus placebo in adolescents

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) or similar (no. of responders)

Follow‐up: 6 weeks

Study population

RR 2
(0.28 to 14.2)

8
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the antioxidant group and the placebo group in adolescents.

250 per 1000

500 per 1000
(70 to 1000)

Moderate

333 per 1000

666 per 1000
(110 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 6 weeks

The mean MGH‐HPS score for the antipsychotic intervention group was 6.83.

The mean reduction of TTM symptom severity in the intervention groups was
5.87 lower
(17.46 lower to 5.72 higher).

6
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the antioxidant group compared to the placebo group on the MGH‐HPS in adolescents.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate

Follow‐up: 6 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

6
(1 study)

⊕⊕⊝⊝
lowb

The evidence is uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).

Figures and Tables -
Summary of findings 2. Antioxidants versus placebo for trichotillomania in adolescents
Summary of findings 3. Antipsychotics versus placebo for trichotillomania in adults

Antipsychotics versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: antipsychotics

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Antipsychotics versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I)

(no. of responders)

Follow‐up: 12 weeks

Study population

RR 5.08
(1.4 to 18.37)

25
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence of benefit on the number of participants who responded to treatment in the antipsychotic group compared to the placebo group.

167 per 1000

847 per 1000
(233 to 1000)

Moderate

167 per 1000

848 per 1000
(234 to 1000)

Reduction of TTM symptom severity
Massachusetts General

Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 12 weeks

The mean MGH‐HPS score for the antipsychotic intervention group was 8.38.

The mean reduction of TTM symptom severity in the intervention group was
4.87 points lower
(8.84 to 0.9 lower).

25
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence for a reduction of TTM symptom severity in the antipsychotic group compared to the placebo group on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate
Follow‐up: 12 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

25
(1 study)

⊕⊕⊝⊝
lowc

The evidence was uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to very small sample size ( < 50).
cDowngraded by two levels due to zero events and very small sample size ( < 50).

Figures and Tables -
Summary of findings 3. Antipsychotics versus placebo for trichotillomania in adults
Summary of findings 4. Cell signal transducers versus placebo for trichotillomania in adults

Cell signal transducers versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: cell signal transducers

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Cell signal transducers versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

Follow‐up: 10 weeks

Study population

RR 1.33
(0.57 to 3.11)

38
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the cell signal transducer group and the placebo group.

316 per 1000

420 per 1000
(180 to 982)

Moderate

316 per 1000

420 per 1000
(180 to 983)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 10 weeks

The mean MGH‐HPS score for the cell signal transducer intervention group was 13.2.

The mean reduction of TTM symptom severity in the intervention groups was
1.3 points lower
(5.12 lower to 2.52 higher).

38
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the cell signal transducer group compared to the placebo group on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate
Follow‐up: 10 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

38
(1 study)

⊕⊕⊝⊝
lowc

The evidence was uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
cDowngraded by two levels due to zero events and very small sample size ( < 50).

Figures and Tables -
Summary of findings 4. Cell signal transducers versus placebo for trichotillomania in adults
Summary of findings 5. Glutamate modulators versus placebo for trichotillomania in adults

Glutamate modulators versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: glutamate modulators

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Glutamate modulators versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

Follow‐up: 12 weeks

Study population

RR 3.5
(1.34 to 9.17)

50
(1 study)

⊕⊕⊕⊝
moderateb

There was moderate‐certainty evidence of benefit on the number of participants who responded to treatment in the glutamate modulator group compared to the placebo group in adults.

160 per 1000

560 per 1000
(214 to 1000)

Moderate

160 per 1000

560 per 1000
(214 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 12 weeks

The mean MGH‐HPS score for the glutamate modulator intervention group was 10.4.

The mean reduction of TTM symptom severity in the intervention groups was
5.6 points lower
(8.5 to 2.7 lower).

50
(1 study)

⊕⊕⊕⊝
moderateb

There was moderate‐certainty evidence for a reduction of TTM symptom severity in the glutamate modulator group compared to the placebo group on the MGH‐HPS in adults.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate
Follow‐up: 12 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

50
(1 study)

⊕⊕⊝⊝
lowc

The evidence was uncertain about the effect of dropouts due to adverse events in adults.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to small sample size (50 to 400).
cDowngraded by two levels due to zero events and small sample size (50 to 400).

Figures and Tables -
Summary of findings 5. Glutamate modulators versus placebo for trichotillomania in adults
Summary of findings 6. Glutamate modulators versus placebo for trichotillomania in children and adolescents

Glutamate modulators versus placebo for trichotillomania in children and adolescents

Patient or population: children and adolescents with trichotillomania
Settings: outpatient
Intervention: glutamate modulators

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Glutamate modulators versus placebo in children and adolescents

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

Follow‐up: 12 weeks

Study population

RR 1.19
(0.37 to 3.77)

39
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence showing no difference in treatment response between the glutamate modulator group and the placebo group in children and adolescents.

211 per 1000

251 per 1000
(78 to 794)

Moderate

211 per 1000

251 per 1000
(78 to 795)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 12 weeks

The mean MGH‐HPS score for the glutamate modulator intervention group was 10.7.

The mean reduction of TTM symptom severity in the intervention groups was
2.83 points lower
(3.76 to 1.9 lower).

39
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence for a potentially large reduction of TTM symptom severity in the glutamate modulator group compared to the placebo group on the MGH‐HPS in children and adolescents.

Tolerability of treatment ‐ dropouts due to adverse eventsc
Dropout rate

Follow‐up: 12 weeks

Study population

RR 2.86
(0.12 to 66.11)

39
(1 study)

⊕⊕⊝⊝
lowd

There was low‐certainty evidence showing no difference in dropouts due to adverse events between groups.

N = 0/19

N = 1/20

Moderate

N = 0/19

N = 1/20

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to very small sample size ( < 50).
cNumbers presented as raw values for N (events) in study population (intervention and control groups), and not modelled on RR.
dDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).

Figures and Tables -
Summary of findings 6. Glutamate modulators versus placebo for trichotillomania in children and adolescents
Summary of findings 7. Opioid antagonists versus placebo for trichotillomania in adults

Opioid antagonists versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: opioid antagonists

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

Opioid antagonists versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders) & NIMH Trichotillomania Severity Scale (NIMH‐TSS)

(no. of responders as > 50% reduction)

Follow‐up: 6 to 8 weeks

Study population

RR 2.14
(0.25 to 18.17)

68
(2 studies)

⊕⊝⊝⊝
very lowb,c

There is very uncertain evidence showing no effect of opioid antagonists on treatment response.

250 per 1000

535 per 1000
(62 to 1000)

Moderate

173 per 1000

370 per 1000
(43 to 1000)

Reduction of TTM symptom severity
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS)

Follow‐up: 8 weeks

The mean MGH‐HPS score for the opioid antagonist intervention group was 12.21.

The mean reduction of TTM symptom severity in the intervention groups was
1.14 points lower
(4.18 lower to 1.9 higher).

51
(1 study)

⊕⊕⊝⊝
lowc

There was low‐certainty evidence showing no difference in reduction of TTM symptom severity in the opioid antagonist group compared to the placebo group on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse events

See comment

See comment

No data available for this outcome.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to moderate heterogeneity (I² = 59%)
cDowngraded by two levels due to wide confidence interval and small sample size (50 to 400).

Figures and Tables -
Summary of findings 7. Opioid antagonists versus placebo for trichotillomania in adults
Summary of findings 8. SSRIs versus placebo for trichotillomania in adults

SSRIs versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: SSRIs

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

SSRIs versus placebo in adults

Treatment response

See comment

See comment

No data available for this outcome.

Reduction of TTM symptom severitya
Massachusetts General Hospital Hair‐Pulling Scale (MGH‐HPS) mean change score

Follow‐up: 12 weeks

The mean change of the MGH‐HPS score for the SSRI intervention group was ‐1.5333.

The mean reduction of TTM symptom severity in the intervention groups was
0.47 points lower
(4.3 lower to 3.36 higher).

31
(1 study)

⊕⊝⊝⊝
very lowb,c,d

The evidence is very uncertain about the effect of SSRIs on reduction of TTM symptom severity on the MGH‐HPS.

Tolerability of treatment ‐ dropouts due to adverse eventse
Dropout rate

Follow‐up: 6 to 12 weeks

Study population

RR 3
(0.33 to 27.62)

78
(2 studies)

⊕⊕⊝⊝
lowf

There was low‐certainty evidence showing no difference in dropouts due to adverse events between groups.

N = 0/39

N = 2/39

Moderate

N = 0/39

N = 2/39

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to serious risk of bias. Concerns with attrition bias. Intention‐to‐treat analysis not used. No reasons for attrition given.
cDowngraded by one level as mean and standard deviations at endpoint were unavailable. Data provided from correspondence were mean change scores from baseline to endpoint.
dDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
eNumbers presented as raw values for N (events) in study population (intervention and control groups), and not modelled on RR.
fDowngraded by two levels due to wide confidence interval and small sample size (50 to 400).

Figures and Tables -
Summary of findings 8. SSRIs versus placebo for trichotillomania in adults
Summary of findings 9. TCAs with predominantly SRI actions versus placebo for trichotillomania in adults

TCAs with predominantly SRI actions versus placebo for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: TCAs with predominantly SRI actions

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

TCAs with predominantly SRI actions versus placebo in adults

Treatment responsea
Clinical Global Impressions ‐ Improvement Scale (CG‐I) (no. of responders)

Follow‐up: 9 weeks

Study population

RR 5.73
(0.36 to 90.83)

16
(1 study)

⊕⊝⊝⊝
very lowb,c

The evidence is very uncertain about the effect of TCAs with predominantly SRI actions on treatment response.

0 per 1000

0 per 1000
(0 to 0)

Moderate

0 per 1000

0 per 1000
(0 to 0)

Reduction of TTM symptom severity
NIMH Trichotillomania Severity Scale (NIMH‐TSS)

Follow‐up: 9 weeks

The mean NIMH‐TSS score for the TCA with predominantly SRI actions intervention group was 9.3.

The mean reduction of TTM symptom severity in the intervention group was
3 points lower
(6.52 lower to 0.52 higher).

16
(1 study)

⊕⊝⊝⊝
very lowb,c

The evidence is very uncertain about the effect of TCAs with predominantly SRI actions on reduction of TTM symptom severity on the NIMH‐TSS.

Tolerability of treatment ‐ dropouts due to adverse eventsd
Dropout rate

Follow‐up: 9 weeks

Study population

RR 4.45
(0.27 to 73.81)

16
(1 study)

⊕⊝⊝⊝
very lowb,c

The evidence is very uncertain about the effect of TCAs with predominantly SRI actions on dropouts due to adverse events.

N = 0/6

N = 3/10

Moderate

N = 0/6

N = 3/10

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by one level due to serious risk of bias. Concerns with attrition bias. Intention‐to‐treat analysis not used, 3 withdrew from clomipramine group due to adverse events. 40% overall attrition rate in clomipramine group.
cDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
dNumbers presented as raw values for N (events) in study population (intervention and control groups), and not modelled on RR.

Figures and Tables -
Summary of findings 9. TCAs with predominantly SRI actions versus placebo for trichotillomania in adults
Summary of findings 10. TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults

TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults

Patient or population: adults with trichotillomania
Settings: outpatient
Intervention: TCAs with predominantly SRI actions

Comparison: placebo

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

No of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

TCAs with predominantly SRI actions versus other TCAs in adults

Treatment responsea
Physician‐rated Clinical

Progress Scale

Follow‐up: 5 weeks

The mean Physician‐rated Clinical Progress Scale score for the TCA with predominantly SRI actions intervention group was 4.7.

The mean treatment response in the intervention group was
4 points lower
(6.13 to 1.87 lower).

26
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence for a beneficial effect on treatment response in the TCAs with predominantly SRI actions group compared to the other TCAs group on the Physician‐rated Clinical Progress Scale.

Reduction of TTM symptom severity
NIMH Trichotillomania Severity Scale (NIMH‐TSS)

Follow‐up: 5 weeks

The mean NIMH‐TSS score for the TCA with predominantly SRI actions intervention group was 10.6

The mean reduction of TTM symptom severity in the intervention groups was
3.8 points lower
(8.08 lower to 0.48 higher).

26
(1 study)

⊕⊕⊝⊝
lowb

There was low‐certainty evidence of no difference in reduction of TTM symptom severity in the TCAs with predominantly SRI actions group compared to the other TCAs group on the NIMH‐TSS.

Tolerability of treatment ‐ dropouts due to adverse events
Dropout rate

Follow‐up: 5 weeks

Differences between groups could not be calculated as there were no dropouts due to adverse events in either group.

Not estimable

26
(1 study)

⊕⊕⊝⊝
lowc

The evidence is uncertain about the effect of dropouts due to adverse events.

*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
CI: confidence interval; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: further research is very unlikely to change our confidence in the estimate of effect.
Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low certainty: we are very uncertain about the estimate.

aResponse is defined as the number of participants with TTM who responded to treatment, as assessed by the CGI‐I or similar.
bDowngraded by two levels due to wide confidence interval and very small sample size ( < 50).
cDowngraded by two levels due to zero events and very small sample size ( < 50).

Figures and Tables -
Summary of findings 10. TCAs with predominantly SRI actions versus other TCAs for trichotillomania in adults
Comparison 1. Antioxidants versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

1.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

36

Risk Ratio (M‐H, Random, 95% CI)

2.25 [0.84, 5.99]

1.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

1.2.1 Clinical Global Impression ‐ Severity Scale (CGI‐S)

1

27

Mean Difference (IV, Random, 95% CI)

‐0.50 [‐1.31, 0.31]

1.2.2 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

27

Mean Difference (IV, Random, 95% CI)

‐1.80 [‐6.22, 2.62]

1.2.3 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

27

Mean Difference (IV, Random, 95% CI)

‐1.00 [‐5.00, 3.00]

1.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

1.3.1 Hamilton Depression Rating Scale (HAM‐D)

1

27

Mean Difference (IV, Random, 95% CI)

0.60 [‐1.82, 3.02]

1.4 Quality of Life ‐ functional disability Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

1.4.1 Sheehan Disability Scale (SDS)

1

27

Mean Difference (IV, Random, 95% CI)

‐0.60 [‐6.53, 5.33]

1.5 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

1.5.1 Dropout rate

1

28

Risk Ratio (M‐H, Random, 95% CI)

Not estimable

Figures and Tables -
Comparison 1. Antioxidants versus placebo in adults
Comparison 2. Antioxidants versus placebo in adolescents

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

2.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

2.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

8

Risk Ratio (M‐H, Random, 95% CI)

2.00 [0.28, 14.20]

2.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

2.2.1 Clinical Global Impression ‐ Severity Scale (CGI‐S)

1

6

Mean Difference (IV, Random, 95% CI)

‐1.13 [‐2.72, 0.46]

2.2.2 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

6

Mean Difference (IV, Random, 95% CI)

‐5.87 [‐17.46, 5.72]

2.2.3 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

6

Mean Difference (IV, Random, 95% CI)

‐2.94 [‐8.14, 2.26]

2.2.4 Trichotillomania Scale For Children ‐ Child Version (TSC‐C)

1

6

Mean Difference (IV, Random, 95% CI)

0.00 [‐1.25, 1.25]

2.2.5 Trichotillomania Scale For Children ‐ Parent Version (TSC‐P)

1

4

Mean Difference (IV, Random, 95% CI)

‐1.20 [‐1.48, ‐0.92]

2.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

2.3.1 Hamilton Depression Rating Scale (HAM‐D)

1

7

Mean Difference (IV, Random, 95% CI)

‐1.62 [‐3.98, 0.74]

2.4 Quality of Life ‐ functional disability Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

2.4.1 Sheehan Disability Scale (SDS)

1

6

Mean Difference (IV, Random, 95% CI)

‐1.30 [‐8.43, 5.83]

2.5 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

2.5.1 Dropout rate

1

8

Risk Ratio (M‐H, Random, 95% CI)

Not estimable

Figures and Tables -
Comparison 2. Antioxidants versus placebo in adolescents
Comparison 3. Antipsychotics versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

3.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

3.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

25

Risk Ratio (M‐H, Random, 95% CI)

5.08 [1.40, 18.37]

3.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

3.2.1 Clinical Global Impressions ‐ Severity Scale (CGI‐S)

1

25

Mean Difference (IV, Random, 95% CI)

‐1.68 [‐2.31, ‐1.05]

3.2.2 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

25

Mean Difference (IV, Random, 95% CI)

‐4.87 [‐8.84, ‐0.90]

3.2.3 Yale‐Brown Obsessive Compulsive Scale for Trichotillomania (TTM‐YBOCS)

1

25

Mean Difference (IV, Random, 95% CI)

‐7.63 [‐12.35, ‐2.91]

3.3 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

3.3.1 Dropout rate

1

25

Risk Ratio (M‐H, Random, 95% CI)

Not estimable

3.4 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

3.4.1 Dry mouth (no. of participants)

1

25

Risk Ratio (M‐H, Random, 95% CI)

13.93 [0.88, 220.37]

3.4.2 Fatigue (no. of participants)

1

25

Risk Ratio (M‐H, Random, 95% CI)

13.93 [0.88, 220.37]

3.4.3 Increased appetite (no. of participants)

1

25

Risk Ratio (M‐H, Random, 95% CI)

12.07 [0.75, 193.73]

3.4.4 Headache (no. of participants)

1

25

Risk Ratio (M‐H, Random, 95% CI)

10.21 [0.62, 167.12]

3.4.5 Weight gain (no. of participants)

1

25

Risk Ratio (M‐H, Random, 95% CI)

10.21 [0.62, 167.12]

Figures and Tables -
Comparison 3. Antipsychotics versus placebo in adults
Comparison 4. Cell signal transducers versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

4.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

4.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

38

Risk Ratio (M‐H, Random, 95% CI)

1.33 [0.57, 3.11]

4.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

4.2.1 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

38

Mean Difference (IV, Random, 95% CI)

‐1.30 [‐5.12, 2.52]

4.2.2 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

38

Mean Difference (IV, Random, 95% CI)

0.00 [‐3.37, 3.37]

4.3 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

4.3.1 Dropout rate

1

38

Risk Ratio (M‐H, Random, 95% CI)

Not estimable

4.4 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

4.4.1 Nausea / upset stomach (no. of participants)

1

38

Risk Ratio (M‐H, Random, 95% CI)

2.00 [0.41, 9.65]

Figures and Tables -
Comparison 4. Cell signal transducers versus placebo in adults
Comparison 5. Glutamate modulators versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

5.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

5.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

50

Risk Ratio (M‐H, Random, 95% CI)

3.50 [1.34, 9.17]

5.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

5.2.1 Clinical Global Impression ‐ Severity Scale (CGI‐S)

1

50

Mean Difference (IV, Random, 95% CI)

‐1.24 [‐1.93, ‐0.55]

5.2.2 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

50

Mean Difference (IV, Random, 95% CI)

‐5.60 [‐8.50, ‐2.70]

5.2.3 Psychiatric Institute Trichotillomania Scale (PITS)

1

50

Mean Difference (IV, Random, 95% CI)

‐6.90 [‐10.56, ‐3.24]

5.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

5.3.1 Hamilton Depression Rating Scale (HAM‐D)

1

50

Mean Difference (IV, Random, 95% CI)

‐0.96 [‐2.88, 0.96]

5.4 Quality of Life ‐ functional disability Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

5.4.1 Sheehan Disability Scale (SDS)

1

50

Mean Difference (IV, Random, 95% CI)

‐2.76 [‐5.58, 0.06]

5.5 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

5.5.1 Dropout rate

1

50

Risk Ratio (M‐H, Random, 95% CI)

Not estimable

Figures and Tables -
Comparison 5. Glutamate modulators versus placebo in adults
Comparison 6. Glutamate modulators versus placebo in children and adolescents

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

6.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

6.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

39

Risk Ratio (M‐H, Random, 95% CI)

1.19 [0.37, 3.77]

6.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

6.2.1 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

39

Mean Difference (IV, Random, 95% CI)

‐2.83 [‐3.76, ‐1.90]

6.2.2 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

39

Mean Difference (IV, Random, 95% CI)

‐1.33 [‐1.97, ‐0.69]

6.2.3 Trichotillomania Scale for Children ‐ Child version (TSC‐C)

1

39

Mean Difference (IV, Random, 95% CI)

‐0.08 [‐0.22, 0.06]

6.2.4 Trichotillomania Scale for Children ‐ Parent version (TSC‐P)

1

39

Mean Difference (IV, Random, 95% CI)

‐0.05 [‐0.16, 0.06]

6.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

6.3.1 Children's Depression Inventory (CDI)

1

39

Mean Difference (IV, Random, 95% CI)

3.10 [1.91, 4.29]

6.4 Tolerability of treatment ‐ Dropouts due to adverse eventsDropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

6.4.1 Dropout rate

1

39

Risk Ratio (M‐H, Random, 95% CI)

2.86 [0.12, 66.11]

6.5 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

6.5.1 Nausea (no. of participants)

1

39

Risk Ratio (M‐H, Random, 95% CI)

0.48 [0.22, 1.01]

Figures and Tables -
Comparison 6. Glutamate modulators versus placebo in children and adolescents
Comparison 7. Opioid antagonists versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

7.1 Treatment response Show forest plot

2

68

Risk Ratio (M‐H, Random, 95% CI)

2.14 [0.25, 18.17]

7.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

51

Risk Ratio (M‐H, Random, 95% CI)

1.04 [0.49, 2.19]

7.1.2 NIMH Trichotillomania Severity Scale (NIMH‐TSS) (no. of responders as >50% reduction)

1

17

Risk Ratio (M‐H, Random, 95% CI)

9.62 [0.57, 161.44]

7.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

7.2.1 Clinical Global Impression ‐ Severity Scale (CGI‐S)

1

51

Mean Difference (IV, Random, 95% CI)

‐0.37 [‐1.10, 0.36]

7.2.2 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS)

1

51

Mean Difference (IV, Random, 95% CI)

‐1.14 [‐4.18, 1.90]

7.2.3 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

51

Mean Difference (IV, Random, 95% CI)

‐0.79 [‐3.62, 2.04]

7.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

7.3.1 Hamilton Depression Rating Scale (HAM‐D)

1

51

Mean Difference (IV, Random, 95% CI)

0.66 [‐1.26, 2.58]

7.4 Quality of Life ‐ functional disability Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

7.4.1 Sheehan Disability Scale (SDS)

1

51

Mean Difference (IV, Random, 95% CI)

‐1.91 [‐5.82, 2.00]

7.5 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

7.5.1 Sedation (no. of participants)

1

51

Risk Ratio (M‐H, Random, 95% CI)

3.12 [0.35, 28.03]

Figures and Tables -
Comparison 7. Opioid antagonists versus placebo in adults
Comparison 8. SSRIs versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

8.1 Treatment response Show forest plot

0

Other data

No numeric data

8.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

8.2.1 Massachusetts General Hospital Hairpulling Scale (MGH‐HPS) mean change score

1

31

Mean Difference (IV, Random, 95% CI)

‐0.47 [‐4.30, 3.36]

8.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

8.3.1 Hamilton Depression Rating Scale (HAM‐D)

1

32

Mean Difference (IV, Random, 95% CI)

0.80 [‐1.90, 3.50]

8.4 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

2

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

8.4.1 Dropout rate

2

78

Risk Ratio (M‐H, Random, 95% CI)

3.00 [0.33, 27.62]

8.5 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

2

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

8.5.1 Nausea (no. of participants)

1

32

Risk Ratio (M‐H, Random, 95% CI)

2.50 [0.57, 11.05]

8.5.2 Insomnia (no. of participants)

1

32

Risk Ratio (M‐H, Random, 95% CI)

0.50 [0.11, 2.35]

8.5.3 Central nervous system or psychiatric effects (nightmares, insomnia, dizziness, irritability, anxiety, feeling of doom) (no. of participants)

1

46

Risk Ratio (M‐H, Random, 95% CI)

1.38 [1.04, 1.83]

8.5.4 GIT effects (no. of participants)

1

46

Risk Ratio (M‐H, Random, 95% CI)

4.67 [1.55, 14.09]

Figures and Tables -
Comparison 8. SSRIs versus placebo in adults
Comparison 9. TCAs with predominantly SRI actions versus placebo in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

9.1 Treatment response Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

9.1.1 Clinical Global Impressions ‐ Improvement Scale (CGI‐I) (no. of responders)

1

16

Risk Ratio (M‐H, Random, 95% CI)

5.73 [0.36, 90.83]

9.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

9.2.1 NIMH Trichotillomania Impairment Scale (NIMH‐TIS)

1

16

Mean Difference (IV, Random, 95% CI)

1.60 [‐0.82, 4.02]

9.2.2 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

16

Mean Difference (IV, Random, 95% CI)

‐3.00 [‐6.52, 0.52]

9.3 Tolerability of treatment ‐ Dropouts due to adverse eventsDropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

9.3.1 Dropout rate

1

16

Risk Ratio (M‐H, Random, 95% CI)

4.45 [0.27, 73.81]

9.4 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

9.4.1 Tremor (no. of participants)

1

16

Risk Ratio (M‐H, Random, 95% CI)

4.45 [0.27, 73.81]

9.4.2 Sedation (no. of participants)

1

16

Risk Ratio (M‐H, Random, 95% CI)

3.18 [0.18, 56.95]

9.4.3 Dry mouth (no. of participants)

1

16

Risk Ratio (M‐H, Random, 95% CI)

3.18 [0.18, 56.95]

9.4.4 Constipation (no. of participants)

1

16

Risk Ratio (M‐H, Random, 95% CI)

3.18 [0.18, 56.95]

Figures and Tables -
Comparison 9. TCAs with predominantly SRI actions versus placebo in adults
Comparison 10. TCAs with predominantly SRI actions versus other TCAs in adults

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

10.1 Treatment response Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

10.1.1 Physician‐rated Clinical Progress Scale

1

26

Mean Difference (IV, Random, 95% CI)

‐4.00 [‐6.13, ‐1.87]

10.2 Reduction of TTM symptom severity Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

10.2.1 NIMH Trichotillomania Impairment Scale (NIMH‐TIS)

1

26

Mean Difference (IV, Random, 95% CI)

‐2.00 [‐3.58, ‐0.42]

10.2.2 NIMH Trichotillomania Severity Scale (NIMH‐TSS)

1

26

Mean Difference (IV, Random, 95% CI)

‐3.80 [‐8.08, 0.48]

10.3 Reduction of comorbid symptoms of depression Show forest plot

1

Mean Difference (IV, Random, 95% CI)

Subtotals only

10.3.1 NIMH Global Assessment Scale for Depression (NIMH‐GASD)

1

26

Mean Difference (IV, Random, 95% CI)

‐0.70 [‐1.60, 0.20]

10.4 Tolerability of treatment ‐ Dropouts due to adverse events Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

10.4.1 Dropout rate

1

26

Risk Ratio (M‐H, Random, 95% CI)

Not estimable

10.5 Tolerability of treatment ‐ Common adverse events (> 20%) Show forest plot

1

Risk Ratio (M‐H, Random, 95% CI)

Subtotals only

10.5.1 Constipation (no. of participants)

1

26

Risk Ratio (M‐H, Random, 95% CI)

0.83 [0.34, 2.06]

10.5.2 Dry mouth (no. of participants)

1

26

Risk Ratio (M‐H, Random, 95% CI)

0.62 [0.28, 1.41]

10.5.3 Tremor (no. of participants)

1

26

Risk Ratio (M‐H, Random, 95% CI)

2.33 [0.77, 7.10]

Figures and Tables -
Comparison 10. TCAs with predominantly SRI actions versus other TCAs in adults