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Study identifier: NCT07616830 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Outcomes of Midline Stoma

Condition: Stoma Colostomy · Stoma Ileostomy  ·  Sponsor: Assiut University

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

* Ileostomy or colostomy is a common surgical procedure used for diverting the lower gastrointestinal content away from distal pathology or anastomotic insufficiency. Once the distal problem has been fixed, the plan is to reverse the stoma. However, the reversal of a stoma is associated with complications, including anastomotic leaks, wound infection, and incisional hernias which can reach up to 33-50%. * The ideal site for a stoma on the abdominal wall depends on several factors, including the patient's anatomy, the type of stoma (colostomy or ileostomy), operative findings, and the patient's preferences. Stomas have traditionally been fashioned through the rectus muscle, away from the midline of the abdomen, and below the umbilicus. * Management of a stoma placed at the center of a long midline laparotomy wound is challenging with the risk of faecal contamination of midline incision. However in many scenarios, the surgeon is left without options rather than to exteriorize the bowel loop through the midline. Moreover, advantages of midline stoma may include: 1. Easy to create and save operative time. 2. Minimize destruction of the anterior abdominal wall (less tissue injury). 3. Eliminate the long-term risk of incisional hernia at the site of previous stoma. Only, few reports assess the outcomes of midline ostomy as a temporary stoma

This description comes directly from the study's public registry record.

Talk to the study team

Mohamad Raafat, MD  ·  0201067877622  ·  mohamad_raafat10@yahoo.com

Faculty of Medicine-Assiut University

Always discuss trial participation with your own doctor first.

Locations (1)

Faculty of Medicine-Assiut UniversityAsyut, Asyut Governorate, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07616830