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Clinical Trial Summary

This is a multi-centered randomized controlled trial of women with stress urinary incontinence or stress predominant mixed urinary incontinence who desire non-surgical therapy.


Clinical Trial Description

In this randomized trial, eligible patients who provide written consent for participation will be enrolled. At enrollment we will collect baseline demographic data and ask participants to complete questionnaires and a 3-day bladder diary. Subjects will be randomized in a 1:1 ratio to continence pessary or disposable intravaginal device. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03174431
Study type Interventional
Source Ohio State University
Contact
Status Completed
Phase N/A
Start date August 1, 2017
Completion date June 1, 2021

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