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Sponsored by: |
University of Cincinnati |
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Information provided by: | University of Cincinnati |
ClinicalTrials.gov Identifier: | NCT00327834 |
The specific aim of this study is to assess the efficacy and safety of atomoxetine compared with placebo in outpatients with binge eating disorder.
Condition | Intervention | Phase |
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Binge-Eating Disorder |
Drug: atomoxetine |
Phase IV |
Study Type: | Interventional |
Study Design: | Randomized, Double-Blind, Placebo Control, Parallel Assignment |
Official Title: | Atomoxetine in the Treatment of Binge Eating Disorder: A Single-Center, Double-Blind, Placebo-Controlled, Flexible Dose Study in Outpatients |
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
United States, Ohio | |
University of Cincinnati Medical Center | |
Cincinnati, Ohio, United States, 45267-0559 |
Principal Investigator: | Susan L: McElroy, MD | University of Cincinnati |
Study ID Numbers: | B4Z-US-X009 |
Study First Received: | May 17, 2006 |
Last Updated: | May 17, 2006 |
ClinicalTrials.gov Identifier: | NCT00327834 |
Health Authority: | United States: Institutional Review Board |
Signs and Symptoms Bulimia Nervosa Signs and Symptoms, Digestive Mental Disorders |
Bulimia Atomoxetine Eating Disorders Hyperphagia |
Neurotransmitter Uptake Inhibitors Neurotransmitter Agents Pathologic Processes Disease Molecular Mechanisms of Pharmacological Action |
Adrenergic Agents Adrenergic Uptake Inhibitors Physiological Effects of Drugs Pharmacologic Actions |