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 type | Observational |
|---|---|
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Asyut) |
| Status | Recruiting |
| Started | December 1, 2023 |
| Main results expected | October 2026 |
| Study ends | December 2026 |
| Registry record updated | July 24, 2024 |
| Trial ID | NCT06517407 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
- Study coordinator: Amira Sayed Mohammed Sayed, Resident
- Email: asmsda1996@gmail.Com
- Phone: 01061434567
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.