Clinical Trials Directory

Trials / Completed

CompletedNCT00414167

Craving, Binge Eating and Obesity

Placebo-Controlled Trial of Bupropion for the Treatment of Binge Eating Disorder

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
61 (actual)
Sponsor
Yale University · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This research study is designed to look at the effectiveness of bupropion for reducing binge eating in overweight persons with binge eating problems. Participants in the study will receive either bupropion or placebo ("sugar" pill, inactive medication) as an outpatient for eight weeks. In addition, participants will be given the option to receive 8 weeks of free behavioral weight loss treatment. This treatment, known to be effective for reducing binge eating and helping people lose weight, will be administered following the medication phase and at no cost. It is expected that compared to placebo, bupropion will produce greater reductions in binge eating.

Detailed description

The proposed study is an 8-week randomized placebo-controlled trial to test the efficacy of bupropion in treating overweight women with binge eating disorder (BED). Bupropion is an antidepressant that has demonstrated efficacy in smoking cessation and some efficacy in obesity treatment. Since cravings and depressed mood are hypothesized to contribute to binge eating episodes, bupropion is a promising psychopharmacological agent in treating binge eating and reducing weight. It is hypothesized that compared to placebo, bupropion will produce significantly greater reductions in the frequency of binge eating. Secondary goals are to explore interrelationships between treatment and changes in cravings, frequency of binge episodes, emotional eating, and weight loss. Following the medication phase of the trial, all patients will be offered 8 weeks of behavioral weight loss treatment administered by doctoral-level psychologists specializing in eating disorders and weight management.

Conditions

Interventions

TypeNameDescription
DRUGbupropion300 mg per day for 8 weeks
OTHERPlaceboPlacebo

Timeline

Start date
2005-12-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2006-12-21
Last updated
2020-04-03
Results posted
2014-03-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00414167. Inclusion in this directory is not an endorsement.