psychiatrist

This work may not be copied, distributed, displayed, published, reproduced, transmitted, modified, posted, sold, licensed, or used for commercial purposes. By downloading this file, you are agreeing to the publisher’s Terms & Conditions.

Original Research

Levetiracetam in Generalized Social Anxiety Disorder: A Double-Blind, Randomized Controlled Trial

Murray B. Stein, MD, MPH; Lakshmi N. Ravindran, MD; Naomi M. Simon, MD, MSc; Michael R. Liebowitz, MD; Arifulla Khan, MD; Olga Brawman-Mintzer, MD; R. Bruce Lydiard, MD, PhD; and Mark H. Pollack, MD

Published: December 15, 2009

Article Abstract

Objective: This multicenter, double-blind, placebo-controlled, 2-arm, parallel-group study was carried out to determine the effectiveness and safety of the novel anticonvulsant levetiracetam for the treatment of generalized social anxiety disorder (GSAD).

Method: After a 1-week, single-blind, placebo run-in period, 217 adult outpatients meeting DSM-IV criteria for social anxiety disorder, generalized type, were randomly assigned (1:1) to 12 weeks of double-blind treatment with either levetiracetam (n‘ ‰=‘ ‰111) or placebo (n‘ ‰=‘ ‰106). Participants were required to have scores of ≥‘ ‰60 on the Liebowitz Social Anxiety Scale (LSAS) and a total score of ≤‘ ‰17 on the 17-item Hamilton Depression Rating Scale (HDRS). The primary outcome measure was mean change from baseline on LSAS total score. Levetiracetam was initiated at 250 mg/d and flexibly titrated up to a maximum dose of 3,000 mg/d (1,500 mg bid). Dosage was held stable for the last 6 weeks of treatment. The study was conducted from September 2003 to June 2004.

Results: No statistically significant difference was found between the adjusted mean changes in LSAS score for levetiracetam (−24.4) and placebo (−28.7) using an efficacy intent-to-treat, last- observation-carried-forward analysis. Rates of response (≥‘ ‰30% reduction in LSAS score) were similar with 41.3% (levetiracetam) and 46.6% (placebo). No significant between-group differences were found on secondary outcome measures, which included changes in Sheehan Disability Scale, Clinical Global Impression of Change, and HDRS scores.

Conclusions: Although well-tolerated, levetiracetam failed to separate from placebo in this trial for the treatment of moderate to severe GSAD.

Submitted: December 12, 2008; accepted February 2, 2009.

Online ahead of print: December 15, 2009.

Corresponding author: Murray B. Stein, MD, MPH, Anxiety and Traumatic Stress Disorders Research Program, University of California San Diego, 8939 Villa La Jolla Drive, Suite 200, La Jolla, CA 92037 (mstein@ucsd.edu).

Volume: 70

Quick Links:

Continue Reading…

Subscribe to read the entire article

$40.00

Buy this Article as a PDF