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Lyrette: Renewing Continence Objective and Subjective Efficacy Study — ROSE  

Stress Urinary Incontinence Clinical Trial

Official title:
Lyrette: Renewing Continence Objective and Subjective Efficacy Study

Clinical Trial Summary

The purpose of this study is to demonstrate the treatment efficacy of the Lyrette® System in women most likely to be treated in an office setting for the condition of stress urinary incontinence, secondary to urethral hypermobility.

Clinical Trial Description

This is a prospective, open-label, single arm clinical study to evaluate the Lyrette System (formerly Renessa System) in a population likely to be treated in a physician's office. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01455779
Study type Interventional
Source Verathon
Contact
Status Unknown status
Phase N/A
Start date September 2011
Completion date July 2015
View Details
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