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Clinical Trial Summary

The purpose of this study is to monitor the long term safety and efficacy of duloxetine in the treatment of severe pure genuine stress incontinence.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00190619
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 3
Start date May 2001
Completion date May 2006

See also
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