drugset / Trial / NCT00327834

Atomoxetine in the Treatment of Binge Eating Disorder

NCT00327834 ↗

RandomizedParallel-groupDouble-blind

Summary

The specific aim of this study is to assess the efficacy and safety of atomoxetine compared with placebo in outpatients with binge eating disorder.

Timeline

Start
2006-05
Primary completion
2007-03
Completion
2007-03

Outcome

Met primary endpoint

paper Compared with placebo (N = 20), atomoxetine (N = 20) was associated with a significantly greater rate of reduction in binge-eating episode frequency PMID 17388708 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Atomoxetine Other / unclassified — —

Indications