drugset / Trial / NCT00174577

Risperidone Augmentation Therapy in Patients Who Have Failed or Only Partially Responded to a Trial of Antidepressant

NCT00174577

RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of risperidone augmentation in patients who have failed to respond or only partially responded to an adequate trial of an antidepressant.

Timeline

Start
2003-02
Primary completion
Completion
2005-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Risperidone Other / unclassified 1 mg
Subject Risperidone Other / unclassified 3 mg