Optimization of Postoperative Bowel Habits - Trial NCT06335797
Access comprehensive clinical trial information for NCT06335797 through Pure Global AI's free database. This phase not specified trial is sponsored by Wake Forest University Health Sciences and is currently Not yet recruiting. The study focuses on Constipation. Target enrollment is 88 participants.
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Study Focus
Sponsor & Location
Wake Forest University Health Sciences
Timeline & Enrollment
N/A
May 01, 2024
Dec 01, 2025
Primary Outcome
Time in hours to first bowel movement comparison between the two arms
Summary
Project is a trial, in which women undergoing vaginal surgery for pelvic organ prolapse will
 be randomized 1:1 to a postoperative bowel regimen of either oral senna or rectal bisacodyl
 suppository.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06335797
Non-Device Trial