Binge-eating Disorder Clinical Trial
Official title:
Atomoxetine in the Treatment of Binge Eating Disorder: A Single-Center, Double-Blind, Placebo-Controlled, Flexible Dose Study in Outpatients
Verified date | June 2011 |
Source | Lindner Center of HOPE |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The specific aim of this study is to assess the efficacy and safety of atomoxetine compared with placebo in outpatients with binge eating disorder.
Status | Completed |
Enrollment | 0 |
Est. completion date | March 2007 |
Est. primary completion date | March 2007 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Subjects will meet the DSM-IV criteria for a diagnosis of binge-eating disorder for at least the last 6 months - In addition, subjects will report at least 3 binge eating episodes per week for the last 6 months prior to randomization Exclusion Criteria: - Have concurrent symptoms of bulimia nervosa or anorexia nervosa - Women who are pregnant, lactating, or of child bearing potential who are not using adequate contraceptive measures - Patients who are displaying clinically significant suicidality or homicidality |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind
Country | Name | City | State |
---|---|---|---|
United States | University of Cincinnati Medical Center | Cincinnati | Ohio |
Lead Sponsor | Collaborator |
---|---|
Lindner Center of HOPE | University of Cincinnati |
United States,
McElroy SL, Guerdjikova A, Kotwal R, Welge JA, Nelson EB, Lake KA, Keck PE Jr, Hudson JI. Atomoxetine in the treatment of binge-eating disorder: a randomized placebo-controlled trial. J Clin Psychiatry. 2007 Mar;68(3):390-8. — View Citation
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