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Recruiting NCT06820359

NCT06820359 Bowel Preparation in Minimally Invasive Gynecologic Surgery

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Clinical Trial Summary
NCT ID NCT06820359
Status Recruiting
Phase
Sponsor Muhammad Aslam
Condition Gynecologic Disease
Study Type INTERVENTIONAL
Enrollment 166 participants
Start Date 2025-02-17
Primary Completion 2026-01-31

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Bowel PreparationNo bowel preparation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 166 participants in total. It began in 2025-02-17 with a primary completion date of 2026-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * 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 Exclusion Criteria: * 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

Contact & Investigator

Central Contact

Muhammad Aslam, MD

✉ maslam2@hfhs.org

📞 313-343-3494

Principal Investigator

Muhammad Aslam, MD

PRINCIPAL INVESTIGATOR

Henry Ford Health

Frequently Asked Questions

Who can join the NCT06820359 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Gynecologic Disease. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06820359 currently recruiting?

Yes, NCT06820359 is actively recruiting participants. Contact the research team at maslam2@hfhs.org for enrollment information.

Where is the NCT06820359 trial being conducted?

This trial is being conducted at Detroit, United States, Warren, United States.

Who is sponsoring the NCT06820359 clinical trial?

NCT06820359 is sponsored by Muhammad Aslam. The principal investigator is Muhammad Aslam, MD at Henry Ford Health. The trial plans to enroll 166 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology