Clinical trial Recruiting at 1 site Observational

Comparing two methods of stoma placement to reduce complications

Official title: Para Rectus Versus Trans Rectus Stoma Placement for Prevention of Stoma Related Complications

Run by Assiut University · NCT06517407 · Data updated 2026-11-12

This study is testing two different ways to place a stoma to see which method helps reduce complications for patients having abdominal surgery.

Quick facts

Study typeObservational
SexAll
Enrollment60 (estimated)
SponsorAssiut University
Academic / other
Locations1 site (Asyut)
StatusRecruiting
StartedDecember 1, 2023
Main results expectedOctober 2026
Study endsDecember 2026
Registry record updatedJuly 24, 2024
Trial IDNCT06517407 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients receiving abdominal enterostomies, whether elective or emergency, at Assiut University Hospital.

Probably not a fit

Patients who have undergone repair of previous abdominal surgery or have known incisional or ventral abdominal hernias may not benefit from this study.

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

What this trial studies

This observational study investigates the impact of stoma placement techniques on the incidence of stoma-related complications. It focuses on patients undergoing abdominal enterostomies at Assiut University Hospital, examining how the location of stoma creation in relation to the rectus abdominis muscle affects outcomes. The study aims to identify factors that may influence complications such as prolapse, retraction, and herniation. By analyzing these factors, the research seeks to improve surgical practices and patient care.

Why it matters

Potential benefit: If successful, this study could lead to improved surgical techniques that reduce complications for patients with stomas.

How similar studies have gone: While the specific approach of this study may be novel, similar studies have indicated that surgical technique can significantly impact stoma-related complications.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* All patient who recieve abdominal enterostomies either elective or emergencies in surgery department of assuit university hospital

Exclusion Criteria:

1. Patient underwent repair of previous abdominal surgery
2. Patient known to have incisional or ventral abdominal hernia

Where it's running

  • Assiut university Hospital
    Asyut, Egypt
    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.
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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.