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The purpose of this study is to compare postoperative outcomes and patient satisfaction between 3 and 6-week postoperative restrictions after a midurethral sling procedure.
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Lead Sponsor
Yale University
Collaborators
NCT03052985 · Pelvic Organ Prolapse, Rectal Prolapse, and more
NCT06376903 · Urinary Stress Incontinence
NCT05464316 · Post-Prostatectomy Incontinence, Urinary Stress Incontinence, and more
NCT02423486 · Urinary Stress Incontinence
NCT03881293 · Urinary Stress Incontinence, Pain
Yale New Haven Hospital
New Haven, Connecticut
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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