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Clinical Trial Summary

Double-blind placebo-controlled study of the biomechanical effects of duloxetine compared with placebo in the treatment of women with pure genuine stress incontinence


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00190567
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 2
Start date October 2001
Completion date April 2006

See also
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