Clinical trial Recruiting at 1 site Observational Ages 18 to 75

How PEG bowel preparation affects gut bacteria in people with or without an appendix

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

Run by Tongji Hospital · NCT07478029 · Data updated 2026-11-12

This observational study will test whether polyethylene glycol colonoscopy prep changes gut bacteria differently in adults who have had an appendectomy compared with those who have not.

Quick facts

Study typeObservational
Ages18 Years to 75 Years
SexAll
Enrollment10 (estimated)
SponsorTongji Hospital
Academic / other
Locations1 site (Wuhan, Hubei)
StatusRecruiting
StartedFebruary 23, 2024
Main results expectedFebruary 23, 2027
Study endsMarch 18, 2027
Registry record updatedMarch 17, 2026
Trial IDNCT07478029 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18–75 years old who are scheduled for colonoscopy, generally healthy, have not used antibiotics in the prior six months, and either have a history of appendectomy/right hemicolectomy or have an intact appendix.

Probably not a fit

People who recently took antibiotics, are pregnant or breastfeeding, have major organ disease or contraindications to colonoscopy, or have significant mental disorders are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This single-center observational study at Tongji Hospital will enroll adults aged 18–75 undergoing colonoscopy and group them by prior appendectomy (or right hemicolectomy) versus intact appendix. Participants will receive standard PEG bowel preparation and provide stool samples before and after the prep for microbiome analysis. The study will compare changes in microbial diversity, shifts in key taxa, and related metabolic markers between the groups while excluding recent antibiotic users and those with major comorbidities or colonoscopy contraindications. The aim is to determine whether the appendix influences microbiome disruption or recovery after PEG bowel cleansing.

Why it matters

Potential benefit: If successful, the findings could clarify whether appendectomy modifies PEG's effects on the gut microbiome and help inform safer colonoscopy preparation practices.

How similar studies have gone: Previous research has shown that PEG bowel preparation produces acute changes in gut microbial diversity and composition, but long-term effects and the specific protective or reservoir role of the appendix remain underexplored.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged 18-75 years.
* Scheduled to undergo colonoscopy.
* Generally healthy without major organ diseases.

  1. For appendectomy group: history of appendectomy or right hemicolectomy (including appendectomy).
  2. For control group: no history of appendectomy or right hemicolectomy.

Exclusion Criteria:

* Allergy or intolerance to PEG laxatives.
* Pregnant or lactating women.
* Mental disorders.
* Use of antibiotics within 6 months prior to study enrollment.

  1. Contraindications to colonoscopy (e.g., severe cardiopulmonary insufficiency).
  2. For control group only: presence of organic diseases.

Where it's running

  • Department of Gastroenterology Tongji Hospital, Tongji Medical college, Huazhong University of Science and technology
    Wuhan, Hubei, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.