← Back to Clinical Trials
Recruiting NCT06550856

NCT06550856 SUTURE-CLOSURE OMENTOPEXY VERSUS OMENTOPEXY ALONE IN REPAIR OF PERFORATED PEPTIC ULCER

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06550856
Status Recruiting
Phase
Sponsor Sohag University
Condition Perforated Peptic Ulcer
Study Type INTERVENTIONAL
Enrollment 50 participants
Start Date 2024-07-15
Primary Completion 2025-05-01

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
SUTURE-CLOSURE OMENTOPEXY IN REPAIR OF PERFORATED PEPTIC ULCEROMENTOPEXY ALONE IN REPAIR OF PERFORATED PEPTIC ULCER

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 50 participants in total. It began in 2024-07-15 with a primary completion date of 2025-05-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The present study will be conducted to assess whether there is a direct benefit associated with modified-Graham's omentopexy (MGO), above and beyond the benefit associated with Graham's omentopexy (GO) in the treatment of perforated duodenal ulcers. We attempted to answer the question whether primary closure of the perforation in MGO will affect the outcome of surgery. Complication rates will be compared for the two alternative surgical procedures.

Eligibility Criteria

Inclusion Criteria: \- All adult patients of both sexes with a clinical diagnosis of perforated peptic ulcer (gastric or duodenal) that are fit to undergo surgery. Exclusion Criteria: \- 1. Patients with associated bleeding ulcer (additional steps are needed to control bleeding). 2\. Patients with associated pathology other than perforated peptic ulcer that needs surgical intervention.

Contact & Investigator

Central Contact

Adel A Abdrabou, Resident

✉ adelosman3399@gmail.com

📞 01014910091

Frequently Asked Questions

Who can join the NCT06550856 clinical trial?

This trial is open to participants of all sexes, studying Perforated Peptic Ulcer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06550856 currently recruiting?

Yes, NCT06550856 is actively recruiting participants. Contact the research team at adelosman3399@gmail.com for enrollment information.

Where is the NCT06550856 trial being conducted?

This trial is being conducted at Sohag, Egypt.

Who is sponsoring the NCT06550856 clinical trial?

NCT06550856 is sponsored by Sohag University. The trial plans to enroll 50 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology