drugset / Trial / NCT00105196

A Study of Aripiprazole in Patients With Major Depressive Disorder

NCT00105196 ↗

RandomizedParallel-groupDouble-blindDiagnostic

Summary

The purpose of this 14 week, randomized, double-blind, placebo controlled study is to assess the safety and efficacy of aripiprazole to placebo as adjunctive treatment to an assigned open-label marketed antidepressant therapy (ADT) in patients with Major Depressive Disorder who demonstrate an incomplete response to a prospective eight week trial of the same assigned open-label marketed antidepressant therapy.

Timeline

Start
2005-03
Primary completion
2008-03
Completion
2008-03

Outcome

Met primary endpoint

registry Aripiprazole + ADT vs Placebo + ADT; p <0.001; Mean Difference (Final Values) -3.73 (95% CI -5.44 to -2.02); t-test, 2 sided NCT00105196 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Aripiprazole Other / unclassified 2 mg Oral
Subject Aripiprazole Other / unclassified 20 mg Oral