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J Clin Psychiatry. 2010 Oct;71(10):1336-43. doi: 10.4088/JCP.09m05114gre. Epub 2010 Apr 20.

A randomized, double-blind, placebo-controlled trial of olanzapine in the treatment of trichotillomania.

Author information

1
Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario, Canada. vanamer@mcmaster.ca

Abstract

BACKGROUND:

Trichotillomania has been considered as part of the obsessive-compulsive disorder spectrum; however, trichotillomania treatment with obsessive-compulsive disorder medications has largely been unsuccessful.

OBJECTIVE:

To determine whether a dopaminergic treatment as used in tics and Tourette's syndrome would be effective in trichotillomania.

METHOD:

Twenty-five participants with DSM-IV trichotillomania participated in a 12-week, randomized, double-blind, placebo-controlled trial of flexible-dose olanzapine for trichotillomania. Recruitment occurred between August 2001 and December 2005, and follow-up was completed in February 2006. The primary outcome measure was the Clinical Global Impressions-Improvement (CGI-I) scale, and secondary measures of efficacy included the Yale-Brown Obsessive Compulsive Scale for Trichotillomania (TTM-YBOCS) and the Clinical Global Impressions-Severity of Illness (CGI-S) scale.

RESULTS:

Eleven of 13 participants (85%) in the olanzapine group and 2 of 12 (17%) in the placebo group were considered responders according to the CGI-I (P = .001). There was a significant change from baseline to end point in the TTM-YBOCS (P < .01) and the CGI-S (P < .001). The mean ± SD dose of olanzapine at end point was 10.8 ± 5.7 mg/d. Twenty-one of 25 patients (84%) reported at least 1 adverse event, but no adverse events resulted in early withdrawal from the study.

CONCLUSION:

Olanzapine seems to be a safe and effective treatment for primary DSM-IV trichotillomania.

TRIAL REGISTRATION:

clinicaltrials.gov Identifier: NCT00182507.

PMID:
20441724
DOI:
10.4088/JCP.09m05114gre
[Indexed for MEDLINE]

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