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Outcomes of Midline Stoma

Outcomes of Midline Stoma: A Prospective Study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07616830
Enrollment
30
Registered
2026-06-01
Start date
2025-06-15
Completion date
2026-09-01
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stoma Colostomy, Stoma Ileostomy

Keywords

stoma, incisional hernia, midline incision

Brief summary

* 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

Detailed description

This is a prospective cohort study

Interventions

PROCEDUREMidline stoma

stoma (ileostomy/colostomy) through midline incision

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who will undergo temporary stoma (ileostomy/colostomy) through midline incision.

Exclusion criteria

* Patients with jejunostomy. * Patients with severe sepsis.

Design outcomes

Primary

MeasureTime frameDescription
Conversion rateDuring surgeryNeed for stoma revision (failure of midline stoma) and creation of conventional trans-rectus stoma.

Secondary

MeasureTime frameDescription
Incidence of peristomal skin complications1 month after surgeryNumber and percentage of patients with peristomal skin complications around stoma including erythema, erosion, ulceration and tissue overgrowth (hypergranulation)
Incidence of Incisional hernia after stoma reversal1 year after surgeryNumber and percentage of patients developing incisional hernia at the previous stoma site (after stoma reversal) confirmed clinically or radiologically (ultrasound or CT)

Countries

Egypt

Contacts

CONTACTMohamad Raafat, MD
mohamad_raafat10@yahoo.com0201067877622
CONTACTFaculty of Medicine-Assiut University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026