Actively Recruiting

Age: 18Years - 75Years
All Genders
Healthy Volunteers
ID07478029

Impact of Polyethylene Glycol (PEG) Bowel Preparation on Intestinal Microbiota Composition and Diversity in Patients Undergoing Appendectomy

Led by Huaping Xie · Updated on 2026-03-17

10

Participants Needed

1

Research Sites

3 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates the impact of polyethylene glycol (PEG) bowel preparation on the gut microbiota in people who have had an appendectomy compared to those who have not. It explores how PEG, commonly used before colonoscopy, may affect intestinal microbes and how the appendix plays a role in protecting and restoring the gut microbiome. The study focuses on the differences in microbial changes and recovery between appendectomy patients and healthy controls over time. Participants will undergo colonoscopy with PEG laxatives used for bowel preparation following standard clinical procedures. Two groups are studied: one with a history of appendectomy or right hemicolectomy including appendectomy, and a control group without such history. Fecal samples will be collected at five time points: before colonoscopy, at the first non-watery stool after colonoscopy, and at one, three, and six months post-colonoscopy for detailed microbial analysis. During the study, participants will provide stool samples and complete questionnaires about their intestinal and general health. Researchers will analyze changes in gut microbes, diversity, and metabolic functions over six months after colonoscopy. Participant identities will be kept confidential, and they can withdraw at any time. The study will share progress updates and individual results with participants throughout the trial.

CONDITIONS

Brief Title

Clinical Study of PEG Bowel Preparation in Appendectomy Patients

Who Can Participate

Age: 18Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-75 years.
  • Scheduled to undergo colonoscopy.
  • Generally healthy without major organ diseases.
  • For appendectomy group: history of appendectomy or right hemicolectomy (including appendectomy).
  • For control group: no history of appendectomy or right hemicolectomy.
Not Eligible

You will not qualify if you...

  • Allergy or intolerance to PEG laxatives.
  • Pregnant or lactating women.
  • Mental disorders.
  • Use of antibiotics within 6 months prior to study enrollment.
  • Contraindications to colonoscopy (e.g., severe cardiopulmonary insufficiency).
  • For control group only: presence of organic diseases.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 6 months

Participants undergo routine colonoscopy preparation with PEG laxatives and fecal samples are collected at multiple time points to monitor gut microbiota changes.

5 sample collection visits: before colonoscopy, first non-watery stool post-colonoscopy, and at 1 month, 3 months, and 6 months post-colonoscopy

Trial Site Locations

Total: 1 location

1

Department of Gastroenterology Tongji Hospital, Tongji Medical college, Huazhong University of Science and technology

Wuhan, Hubei, China, 430030

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Research Team

P

ping h Xie

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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