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The study design will be a cohort study to determine the incidence of FI symptoms at 6, 12 and 24 weeks postpartum in primiparous women sustaining an OASI. At 6, 12 and 24 weeks postpartum, subjects w...
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Lead Sponsor
NICHD Pelvic Floor Disorders Network
Collaborators
NCT05396456 · Fecal Incontinence
NCT05626816 · Fecal Incontinence
NCT06532123 · Fecal Incontinence
NCT06754189 · Urinary Incontinence, Urinary Incontinence, Urge, and more
NCT06562140 · Colorectal Cancer, Anal Cancer, and more
University of Alabama at Birmingham
Birmingham, Alabama
University of California San Diego
La Jolla, California
Loyola University
Maywood, Illinois
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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