Clinical trial Recruiting at 1 site Interventional Ages 18 to 75

Parastomal Hernia After Mesenteric Molding Suturing in Colostomy

Official title: A Prospective Randomized Controlled Trial Comparing the Incidence of Parastomal Hernia After Mesenteric Molding Suturing and Non-molding Suturing in Colostomy Surgery

Run by The First Affiliated Hospital with Nanjing Medical University · NCT06674187 · Data updated 2026-11-12

This study tests whether mesenteric molding suturing reduces parastomal hernias after colostomy compared with non-molding suturing in adults.

Quick facts

Study typeInterventional
Ages18 Years to 75 Years
SexAll
Enrollment234 (estimated)
SponsorThe First Affiliated Hospital with Nanjing Medical University
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Nanjing, Jiangsu)
StatusRecruiting
StartedDecember 1, 2024
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedJuly 28, 2026
Trial IDNCT06674187 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 and older undergoing colostomy who can consent and are expected to survive more than one year without major organ dysfunction.

Probably not a fit

Patients with recent major abdominal surgery, pregnancy, major immunosuppression, or conditions preventing informed consent may not benefit.

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

What this trial studies

This interventional study compares two suturing techniques used during colostomy surgery to see if mesenteric molding suturing lowers the rate of parastomal hernia. Eligible adults undergoing colostomy will be assigned to regular mesenteric molding suturing or a non-molding technique. The study focuses on postoperative development of parastomal hernia and may inform best surgical practice to prevent this complication. Outcomes will be measured over a defined follow-up period to assess incidence and safety. Conducted at the First Affiliated Hospital with Nanjing Medical University, the trial aims to clarify whether a technical modification at the time of stoma creation can reduce PSH risk.

Why it matters

Potential benefit: If successful, this approach could reduce the risk of parastomal hernia and related complications for patients undergoing colostomy.

How similar studies have gone: Previous research on techniques to prevent parastomal hernia has shown variable results; this study evaluates a specific suturing modification that is not yet proven in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or older.
* Patients requiring colostomy surgery.
* Ability to provide written informed consent.
* Expected survival of more than one year.
* No severe comorbidities such as heart, lung, liver, or kidney dysfunction.

Exclusion Criteria:

* Pregnant or breastfeeding women.
* History of major abdominal surgery that could affect the development of PSH.
* Mental illness that impairs understanding of the study content and ability to give informed consent.
* Patients receiving immunosuppressive therapy or chemotherapy.

Where it's running

  • First Affiliated Hospital of Nanjing Medical University
    Nanjing, Jiangsu, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.