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

Publications

Drugs

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