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A Duloxetine Dosing Strategy Study in Korean Patients With Major Depressive Disorder

Major Depressive Disorder (MDD) Clinical Trial

Official title:
A Phase 4 Comparison of Duloxetine Dosing Strategies in the Treatment of Korean Patients With Major Depressive Disorder

Clinical Trial Summary

The purpose of this study is to assess nausea severity in response to four different drug dosing strategies of Duloxetine (30 mg with food, 60 mg with food, 30 mg without food, and 60 mg without food) in Korean patients with major depressive disorder (MDD).

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00960986
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 4
Start date August 2009
Completion date April 2011
View Details
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