Clinical Trial

Pediatric Colostomy Reversal: Traditional Care vs. Enhanced Recovery After Surgery

Recruiting
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Record status
This record was last updated October 3, 2025 (before its estimated November 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this clinical trial is to learn whether using an Enhanced Recovery After Surgery (ERAS) protocol helps children recover faster after colostomy reversal compared with traditional care. The main question it aims to answer is: Does ERAS lower the number of days children need to stay in the hospital after colostomy reversal compared with traditional care? Researchers will compare two groups: ERAS group - Children receive shorter pre-surgery fasting, no mechanical bowel preparation, early pain control, and early feeding after surgery. Traditional care group - Children receive the usual long bowel preparation, overnight fasting, opioid pain medicine, and a longer period without food after surgery. Participants will: Be randomly assigned to either the ERAS or traditional care group Have their colostomy surgically closed by experienced pediatric surgeons Be monitored daily until they can eat a solid meal without vomiting; this marks the end of their hospital stay The study will enroll 60 children ages 2-13 at Children's Hospital Faisalabad, Pakistan. Researchers will measure length of hospital stay from surgery until discharge as the main outcome.
Trial Details
NCT Number NCT07206836
Lead Sponsor Children Hospital Faisalabad
Conditions Colostomy - Stoma, Stoma Reversal Procedure, ERAS
Enrollment 60 participants
Start Date 2025-08-01
Primary Completion 2025-11 (estimated)
Study Completion 2025-11 (estimated)
Updated on ClinicalTrials.gov 2025-10-03