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Clinical Trial Summary

This study aims to evaluate safety and benefits of early oral feeding compared to traditional delayed oral feeding in patients undergoing perforated peptic ulcer repairs. Study population & Sample size :(


Clinical Trial Description

Study Design: This study is a single-center, prospective, parallel arm, randomized controlled trial. Patients will be randomly assigned in 1:1 ratio to receive either delayed oral feeding or early oral feeding. Methods: Patients will be randomly assigned into two groups. Group A patients followed an early oral feeding protocol(12 hours), and Group B received delayed oral feeding (72 hours). Outcome parameter : The outcomes are incidence of postoperative complications including Postoperative repair leakage, Infection-related postoperative complications , Number of days of hospital stay and return of bowel function and Diet intolerance. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06042933
Study type Interventional
Source Cairo University
Contact mohammed elshwadfy
Phone 00201025524630
Email m.elshwadfy1988@gmail.com
Status Recruiting
Phase N/A
Start date March 2, 2023
Completion date November 1, 2023

See also
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Completed NCT04194060 - ERAS vs Conventional Approach in Peptic Perforation-RCT N/A
Recruiting NCT04447170 - Laparoscopic Versus Open Repair of Peptic Ulcer Perforation
Completed NCT05489497 - Morbidity After Surgical Treatment of Perforated Ulcer