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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
NCT05626816 · Fecal Incontinence
NCT06532123 · Fecal Incontinence
NCT04506593 · Eosinophilic Esophagitis, Gastroesophageal Reflux Disease (GERD), and more
NCT05771597 · Fecal Incontinence, Dyssynergic Defecation, and more
NCT03825575 · Fecal Incontinence
University of Alabama at Birmingham
Birmingham, Alabama
University of California San Diego
La Jolla, California
Loyola University
Maywood, Illinois
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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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