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Clinical Trial Summary

The study is designed to assess efficacy and subject satisfaction of two sling devices: Advance and Argus, in male patients with stress urinary incontinence after prostatectomy.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01866085
Study type Interventional
Source Jewish General Hospital
Contact Jacques Corcos, MD
Phone 1-514-340-8222
Email jcorcos@jgh.mcgill.ca
Status Recruiting
Phase N/A
Start date June 2012
Completion date June 2015

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