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NCT07147062

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

Recruiting now NA Last updated 9 September 2025
What this trial tests

NA trial testing Rectus Sheath Block in Percutaneous Internal Ring Suturing in 65 participants. Currently enrolling.

Timeline
8 September 2025
Primary endpoint
13 February 2026
27 February 2026

Quick facts

Lead sponsorDiskapi Yildirim Beyazit Education and Research Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment65
Start date8 September 2025
Primary completion13 February 2026
Estimated completion27 February 2026
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Diskapi Yildirim Beyazit Education and Research Hospital

Who can join

Adults 1 to 8, any sex, with Percutaneous Internal Ring Suturing or Pain Management. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Rectus Sheath Block

Trials testing the same drug.

Other Diskapi Yildirim Beyazit Education and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07147062.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing