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The purpose of this research study is to better understand optimal restrictions for patients postoperatively following a mesh urethral sling placement for patients with stress urinary incontinence. P...
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Lead Sponsor
University of Iowa
NCT07208682 · Bladder Perforation, Retropubic Midurethral Sling, and more
NCT06724133 · Search MeSH
NCT04967976 · Breast Cancer, Radiation, and more
NCT07539558 · Had Undergone a Hysterectomy, Had Not Been Diagnosed With Cancer, and more
NCT07386067 · Mesh, Inguinal Hernia
University of Iowa Health Care
Iowa City, Iowa
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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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