The American Journal of Psychiatry
Journal Home Search Current Issue Past Issues Subscribe All APPI Journals Help Contact Us
 
Am J Psychiatry 164:1242-1249, August 2007
doi: 10.1176/appi.ajp.2007.06060981
© 2007 American Psychiatric Association
Quicksearch
Advanced Search
Or Search All APPI Journals
This Article
* Full Text
* Full Text (PDF)
* Alert me when this article is cited
* Alert me if a correction is posted
* Citation Map
Services
* Email this article to a Colleague
* Similar articles in this journal
* Similar articles in PubMed
* Alert me to new issues of the journal
* Add to My Articles & Searches
* Download to citation manager
* reprints & permissions
Citing Articles
* Citing Articles via HighWire
* Citing Articles via Google Scholar
Google Scholar
* Articles by Frye, M. A.
* Articles by Post, R. M.
* Search for Related Content
PubMed
* PubMed Citation
* Articles by Frye, M. A.
* Articles by Post, R. M.
Related Collections
* Bipolar Disorder
* Other Somatic Therapy
*Related Article

A Placebo-Controlled Evaluation of Adjunctive Modafinil in the Treatment of Bipolar Depression

Mark A. Frye, M.D., Heinz Grunze, M.D., Trisha Suppes, M.D., Ph.D., Susan L. McElroy, M.D., Paul E. Keck Jr., M.D., Jorge Walden, M.D., Gabriele S. Leverich, M.S.W., L.C.S.W.-C., Lori L. Altshuler, M.D., Shoshanna Nakelsky, M.P.H., Sun Hwang, M.S., Jim Mintz, Ph.D., and Robert M. Post, M.D.

OBJECTIVE: Modafinil is approved by the U.S. Food and Drug Administration for improving wakefulness in patients with excessive sleepiness associated with narcolepsy, obstructive sleep apnea, and shift-work sleep disorder. This study was conducted to evaluate the efficacy and safety of adjunctive modafinil in bipolar depression, which is often characterized by excessive sleepiness and fatigue. METHOD: Eighty-five patients with bipolar depression that was inadequately responsive to a mood stabilizer with or without concomitant antidepressant therapy were randomly assigned to receive adjunctive modafinil (N=41) or placebo (N=44) for 6 weeks. The primary outcome measure was baseline-to-endpoint change in score on the Inventory of Depressive Symptoms—Clinician Rated (IDS). RESULTS: The baseline-to-endpoint change in IDS score was significantly greater in the modafinil group (mean dose, 177 mg/day) compared with the placebo group. Improvement in depressive symptoms was significantly greater in the modafinil group by week 2, and this greater improvement was maintained at weeks 4, 5, and 6. Both the response and remission rates were significantly higher in the modafinil group (44% and 39%) compared with the placebo group (23% and 18%). During the 6-week study period, there was no difference between groups in treatment-emergent hypomania or mania (six patients in the modafinil group and five in the placebo group) or hospitalization for mania (one in each group). CONCLUSIONS: These data suggest that adjunctive modafinil at doses of 100–200 mg a day may improve depressive symptoms in patients with bipolar disorder.


Related Article:

In This Issue
Am J Psychiatry 2007 164: 36. [Full Text] [PDF]



This article has been cited by other articles:


Home page
Am. J. PsychiatryHome page
D. T. PLANTE
Treatment-Emergent Hypomania or Mania With Modafinil
Am J Psychiatry, January 1, 2008; 165(1): 134 - 135.
[Full Text] [PDF]


Home page
JWatch PsychiatryHome page
A New Treatment Approach for Bipolar Depression
Journal Watch Psychiatry, September 24, 2007; 2007(924): 1 - 1.
[Full Text]




Get information about faster international access.

Privacy Policy

Copyright © 2007 American Psychiatric Association. All rights reserved.

Home | Search | Current Issue | Past Issues | Subscribe | All APPI Journals | Help | Contact Us

American Psychiatric Publishing, Inc. American Psychiatric Association
1000 Wilson Boulevard, Suite 1825, Arlington, VA 22209-3901 * 800-368-5777 * appi at psych.org