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Meta-Analysis
. 1995 Jan;52(1):53-60.
doi: 10.1001/archpsyc.1995.03950130053006.

Efficacy and tolerability of serotonin transport inhibitors in obsessive-compulsive disorder. A meta-analysis

Affiliations
Meta-Analysis

Efficacy and tolerability of serotonin transport inhibitors in obsessive-compulsive disorder. A meta-analysis

J H Greist et al. Arch Gen Psychiatry. 1995 Jan.

Abstract

Background: Questions have been raised regarding the relative efficacy and tolerability of the different serotonin transport inhibitors in the treatment of obsessive-compulsive disorder. We compared the results from four large multicenter placebo-controlled trials of the serotonin transport inhibitors clomipramine hydrochloride (N = 520), fluoxetine hydrochloride (N = 355), fluvoxamine maleate (N = 320), and sertraline hydrochloride (N = 325) for the treatment of obsessive-compulsive disorder.

Methods: Effect size was calculated by subtracting the end-point drug treatment mean change from the end-point placebo mean change and dividing by the end-point pooled change standard deviation. A test for overall differences between effect sizes was conducted, followed by all possible pairwise comparisons. The Yale-Brown Obsessive Compulsive Scale was the primary outcome measure for all four studies.

Results: All four agents were significantly more effective than placebo, with clomipramine significantly more effective than the other three treatments, which did not differ in effect size. A significantly greater percentage of patients treated with clomipramine were rated much or very much improved than were patients treated with fluoxetine, fluvoxamine, or sertraline.

Conclusion: While the results of this meta-analysis support the superiority of clomipramine, head-to-head, double-blind comparisons of these compounds would be the best test of comparative efficacy and tolerability.

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  • Venlafaxine in obsessive-compulsive disorder.
    Yaryura-Tobias JA, Neziroglu FA. Yaryura-Tobias JA, et al. Arch Gen Psychiatry. 1996 Jul;53(7):653-4. doi: 10.1001/archpsyc.1996.01830070103016. Arch Gen Psychiatry. 1996. PMID: 8660133 Clinical Trial. No abstract available.

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