Optimization of Postoperative Bowel Habits
Recruiting
N/A
Interventional Study
Constipation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 88 (estimated)
- Sponsor
- Wake Forest University Health Sciences · Other
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About This Trial
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.
Trial Locations
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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 …
Contacts