Outcomes of Different Surgical Procedures After High Level Resection for Patients With Small Intestinal Gangrene
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssiut University
About this trial
In this cohort study, aim to evaluate and compare short-term postoperative outcomes of different surgical procedures for patients with intestinal gangrene who underwent high level small bowel resection (\< 150 cm from DJ).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1) Distance of proximal resection margin less than 150 cm from DJ. 2) Mesenteric vascular ischemia. 3) Strangulating obstruction e.g. due to hernia, volvulus, band, etc.
Disqualifiers
1) Patients less than 18 years. 2) Patients with malignant disease. 3) Patients with almost all small bowel loops resected (< 60 cm remaining).
Trial population
This study is a prospective non-randomized comparative study. Patients who will undergo high level small bowel resection for intestinal gangrene during the period from September 2024 to September 2026 are included.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
40 Participants
are grouped into 4 trial groupsGroup A: Group A: Primary anastomosis: using hand sewing technique
Group B: Group B: Primary anastomosis with prophylactic tube enterostomy. Feeding jejunostomy may be inserted
Group C: Group C: Jejunostomy: double barrel stoma.
Group D: Group D: Jejunostomy: double barrel stoma with distal refeeding via the mucous fistula opening.
Trial outcomes
Primary outcomes
1
morality rate
Time frame
within 90 days of surgeryLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: