Clinical Trial

Comparison of the Postoperative Analgesic Effects of RSB and CEB in Pediatric Patients Scheduled for Percutaneous Internal Ring Suturing

Recruiting
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Record status
This record was last updated September 9, 2025 (before its estimated February 13, 2026 completion). Its status may not reflect the trial's current state.
Summary
Inguinal hernia is one of the most common surgical pathologies in children, and the minimally invasive percutaneous internal ring suturing (PIRS) technique is widely preferred. By providing effective pain control, nerve blocks reduce postoperative opioid requirements, thereby minimising opioid-related adverse effects and lowering the risk of pulmonary and cardiovascular complications. This study aims to compare the postoperative analgesic effects of rectus sheath block and caudal epidural block in pediatric patients undergoing PIRS.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-08-21.
Status change: Not Yet Recruiting → Recruiting 2025-09-08
Trial Details
NCT Number NCT07147062
Lead Sponsor Diskapi Yildirim Beyazit Education and Research Hospital
Conditions Percutaneous Internal Ring Suturing, Pain Management
Enrollment 65 participants
Start Date 2025-09-08
Primary Completion 2026-02-13 (estimated)
Study Completion 2026-02-27 (estimated)
Updated on ClinicalTrials.gov 2025-09-09