Bowel Preparation in Minimally Invasive Gynecologic Surgery
Recruiting now · Not applicable
Conditions studied: Gynecologic Disease
In brief
This is a prospective randomized study of patients who are scheduled to undergo minimally invasive robotic gynecologic surgery. Patients will be randomized to require either pre-surgical bowel preparation vs. no bowel preparation. The effect of bowel preparation on intraoperative visualization, bowel handling, intestinal load and ease of surgery will be assessed. Patient comfort and satisfaction will be assessed.
Key facts
- Study ID
- NCT06820359
- Run by
- Muhammad Aslam
- People needed
- 166
- Starts
- 2025-02-17
- Expected to finish
- 2026-01-31
- Last updated by the study team
- 2025-02-11
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Scheduled to undergo minimally invasive robotic gynecologic surgery;
- Age 18 years and above
- Willing to perform an enema if randomized to the enema group
- Able to read and understand English
- Willing to sign an informed consent form
You may not qualify if…
- Scheduled for open surgery
- Younger than 18 years of age
- Unwilling to perform an enema if randomized to the enema group
- Unable to read and understand English
- Unwilling to sign an informed consent form
Where it is running
- Henry Ford St. John Hospital — Detroit, Michigan, United States (enrolling)
- Henry Ford Macomb-Oakland Hospital, Warren Campus — Warren, Michigan, United States (enrolling)
Full record on ClinicalTrials.gov
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