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The purpose of this study is to determine if there is a difference in post-operative voiding function between subjects receiving local anesthetic and those receiving placebo at the time of mid-urethra...
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Lead Sponsor
University of Massachusetts, Worcester
NCT06706362 · Stress Urinary Incontinence
NCT06862648 · Stress Urinary Incontinence (SUI)
NCT05616481 · Stress Urinary Incontinence, Burch Colposuspention
NCT06933407 · Urinary Incontinence, Urinary Incontinence, Stress, and more
NCT06840093 · Postoperative Restriction, Midurethral Sling, and more
University of Massachusetts
Worcester, Massachusetts
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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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