drugset / Trial / NCT00149799

Effectiveness of Escitalopram in the Treatment of Body Dysmorphic Disorder

NCT00149799 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

This study's primary aim is to compare time to relapse and relapse rates in responders to acute escitalopram who are then randomized to placebo versus continuation treatment with escitalopram.

Timeline

Start
2005-05
Primary completion
2013-03
Completion
2013-03

Outcome

Met primary endpoint

registry Phase II: Escitalopram vs Phase II: Placebo; p = 0.048; Hazard Ratio (HR) 2.73 (95% CI 1.01 to 8.59); Regression, Cox NCT00149799 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Escitalopram Small molecule 30 mg —