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Topiramate Augmentation in Refractory Obsessivecompulsive Disorder: A Randomized, Double-Blind, Placebo-Controlled Trial



Afshar H1 ; Akuchekian S2 ; Mahaky B3 ; Zarean E4
Authors
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Authors Affiliations
  1. 1. Psychosomatic Research Center, Department of Psychiatry, School of Medicinee, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Behavioral Sciences Research Center, Nour Hospital, Department of Psychiatry, School of Medicinee, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Biostatistics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Behavioral Sciences Research Center, Nour Hospital, Department of Psychiatry, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Journal of Research in Medical Sciences Published:2014

Abstract

Background: This study aimed to assess the efficacy of topiramate, a glutamate-modulating agent, in patients with treatment-resistant obsessive-compulsive disorder (OCD) as an adjunct to serotonin reuptake inhibitors (SRIs).; Materials and Methods: Thirty-eight patients with refractory OCD, were randomly assigned to receive topiramate or placebo. This study was designed as a 12 weeks, double-blind, placebo-controlled trial. Primary outcome measures were the change in Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) score and the rate of treatment response in each group at the study end point. Treatment response was considered as 25% or more reduction in Y-BOCS score.; Results: A total of 13 patients in the topiramate group and 14 ones in the placebo group completed the trial. Topiramate-assigned patients showed significantly improved mean Y-BOCS score over time (P < 0.001). Although differences between two groups were significant in the Y-BOCS score at the first 2 months (P = 0.01), this was not significant at the end of the study (P = 0.10). Changes of Clinical Global Impression (CGI)-Severity of Illness Scale score and CGI-Improvement Scale score were not significantly different between two groups (P > 0.05). Treatment response was almost significantly different in the topiramate group comparing placebo group (P = 0.054). Mean topiramate dosage was 137.5 mg/day (range, 100-200).; Conclusion: This study didn’t show efficacy of topiramate as an agent to augment SRIs in treatment-resistant OCD patients. © 2014, Isfahan University of Medical Sciences(IUMS). All rights reserved.
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