NCT07147062 Comparison of the Postoperative Analgesic Effects of RSB and CEB in Pediatric Patients Scheduled for Percutaneous Internal Ring Suturing
| NCT ID | NCT07147062 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Diskapi Yildirim Beyazit Education and Research Hospital |
| Condition | Percutaneous Internal Ring Suturing |
| Study Type | INTERVENTIONAL |
| Enrollment | 65 participants |
| Start Date | 2025-09-08 |
| Primary Completion | 2026-02-13 |
Eligibility & Interventions
Eligibility Fast-Check
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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 65 participants in total. It began in 2025-09-08 with a primary completion date of 2026-02-13.
⚠ 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
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.
Eligibility Criteria
Inclusion Criteria: * Patients aged between 1 and 8 years * ASA physical status I-II * Patients who underwent PIRS surgery in the operating room and received either a rectus sheath block or a caudal epidural block Exclusion Criteria: * Patients younger than 1 year or older than 8 years * ASA physical status ≥ III * History of bleeding diathesis
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07147062 clinical trial?
This trial is open to participants of all sexes, aged 1 Year or older, up to 8 Years, studying Percutaneous Internal Ring Suturing. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07147062 currently recruiting?
Yes, NCT07147062 is actively recruiting participants. Contact the research team at elifsule-91@hotmail.com for enrollment information.
Where is the NCT07147062 trial being conducted?
This trial is being conducted at Altındağ, Turkey (Türkiye).
Who is sponsoring the NCT07147062 clinical trial?
NCT07147062 is sponsored by Diskapi Yildirim Beyazit Education and Research Hospital. The trial plans to enroll 65 participants.