
J Neuropsychiatry Clin Neurosci 20:178-184, May 2008
doi: 10.1176/appi.neuropsych.20.2.178
© 2008 American Neuropsychiatric Association
Double-Blind Randomized Treatment of Poststroke Depression Using Nefiracetam
Robert G. Robinson, M.D.,
Ricardo E. Jorge, M.D. and
Kathleen Clarence-Smith, M.D., Ph.D.
Received February 2, 2007; revised April 12, 2007; accepted April 16, 2007. Drs. Robinson and Jorge are affiliated with the Department of Psychiatry at the Carver College of Medicine, The University of Iowa, in Iowa City, Iowa; Dr. Clarence-Smith is affiliated with CSK-Consulting in Washington, D.C. Address correspondence to Robert G. Robinson, M.D., Department of Psychiatry, The University of Iowa, 200 Hawkins Dr., Iowa City, IA 52242; robert-robinson{at}uiowa.edu (e-mail).
In preliminary trials, nefiracetam, a gamma aminobutyric compound, enhanced blood flow and improved mood following stroke. Within 3 months following stroke with major depression, 159 patients were enrolled in a double-blind trial of nefiracetam or placebo. Repeated measures analysis of covariance failed to show a significant time-by-treatment interaction. Response rates were greater than 70% and remission rates were greater than 40% for nefiracetam and placebo. The top quintile of Hamilton Depression Rating Scale scores showed significant effect after 900 mg of nefiracetam versus 600 mg or placebo. Nefiracetam was not an effective treatment for poststroke depression but produced significant improvement in the most severely depressed patients.
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