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Post Market Study Of Single Incision Sling Versus Transobturator Sling for Stress Urinary Incontinence — Solyx  

Stress Urinary Incontinence Clinical Trial

Official title:
A Prospective, Non-Randomized, Parallel Cohort, Multi-center Study of the Solyx™ Single Incision Sling System vs. the Obtryx™ II Sling System for the Treatment of Women With Stress Urinary Incontinence

Clinical Trial Summary

The purpose of this research study is to compare the treatment device (Solyx) to a different mesh sling or control device (Obtryx II) for the treatment of symptoms for Stress Urinary Incontinence (SUI). Safety information and patient outcomes will be collected for three (3) years and evaluated.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01784588
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date January 17, 2018
View Details
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