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BRL29060A (Paroxetine Hydrochloride Hydrate) in Posttraumatic Stress Disorder

Post-Traumatic Stress Disorder Clinical Trial

Official title:
BRL29060A in Posttraumatic Stress Disorder

Clinical Trial Summary

This was a 52-week, non-comparative, uncontrolled study of paroxetine in Japanese PTSD patients to obtain clinical experience regarding efficacy and safety. In this study, subjects received paroxetine 20mg-40mg once daily after an evening meal.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00839397
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 3
Start date May 2002
Completion date June 2005
View Details
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