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Atomoxetine in the Treatment of Binge Eating Disorder
This study has been completed.
Sponsored by: University of Cincinnati
Information provided by: University of Cincinnati
ClinicalTrials.gov Identifier: NCT00327834
  Purpose

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
Binge-Eating Disorder
Drug: atomoxetine
Phase IV

MedlinePlus related topics: Eating Disorders
Drug Information available for: Atomoxetine Atomoxetine hydrochloride
U.S. FDA Resources
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
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00327834

Locations
United States, Ohio
University of Cincinnati Medical Center
Cincinnati, Ohio, United States, 45267-0559
Sponsors and Collaborators
University of Cincinnati
Investigators
Principal Investigator: Susan L: McElroy, MD University of Cincinnati
  More Information

Publications indexed to this study:
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

Study placed in the following topic categories:
Signs and Symptoms
Bulimia Nervosa
Signs and Symptoms, Digestive
Mental Disorders
Bulimia
Atomoxetine
Eating Disorders
Hyperphagia

Additional relevant MeSH terms:
Neurotransmitter Uptake Inhibitors
Neurotransmitter Agents
Pathologic Processes
Disease
Molecular Mechanisms of Pharmacological Action
Adrenergic Agents
Adrenergic Uptake Inhibitors
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 14, 2009