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Optimization of Postoperative Bowel Habits
Recruiting
Optimization of Postoperative Bowel Habits Following Pelvic Reconstructive Surgery: a Randomized Controlled Trial
Who can join
Ages 18 and older · Women
Full eligibility criteria
Inclusion Criteria: * Women ages 18 and older scheduled to undergo vaginal pelvic organ prolapse repair Exclusion Criteria: * Women younger than 18 years old * Those unable to provide consent * Preexisting chronic laxative use * Conditions that could affect bowel function including, inflammatory bowel disease, irritable bowel syndrome, colorectal cancer, rectovaginal fistula; concurrent bowel surgery; intraoperative bowel injury
About the study
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.
What is being tested
- Senna Tab (dietary supplement)
- Dulcolax Suppositories (dietary supplement)
Sponsor: Wake Forest University Health Sciences · Participants: 88 · Started: Oct 16, 2024
Contact the study team
- Christina M Mezes, MD · Phone: 336-713-4098
- Sachin N Vyas, MS, PhD · Phone: 336-713-4098
Official record on ClinicalTrials.gov — NCT06335797
Locations in the U.S.
| North Carolina | Wake Forest University Health Sciences, Winston-Salem |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.