Comparing two methods of stoma placement to reduce complications
Para Rectus Versus Trans Rectus Stoma Placement for Prevention of Stoma Related Complications
Assiut University · NCT06517407
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 |
|---|---|
| Enrollment | 60 (estimated) |
| Sex | All |
| Sponsor | Assiut University (other) |
| Locations | 1 site (Asyut) |
| Trial ID | NCT06517407 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates include patients receiving abdominal enterostomies, whether elective or emergency, at Assiut University Hospital.
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.
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 performed: While the specific approach of this study may be novel, similar studies have indicated that surgical technique can significantly impact stoma-related complications.
Eligibility criteria
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 this trial is running
Asyut
- Assiut university Hospital — Asyut, Egypt (RECRUITING)
Study contacts
- Study coordinator: Amira Sayed Mohammed Sayed, Resident
- Email: asmsda1996@gmail.Com
- Phone: 01061434567
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Stoma Malfunction