RecruitingNCT07762339

Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy: A Prospective Observational Study

Comparison of Erector Spinae Plane Block and Caudal Block for Postoperative Analgesia in Pediatric Patients Undergoing Orchiopexy


Sponsor

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Enrollment

84 participants

Start Date

Jun 8, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This study aims to compare the analgesic efficacy of ultrasound-guided erector spinae plane block and caudal block for postoperative pain management in pediatric patients undergoing orchiopexy. Postoperative pain scores, time to first rescue analgesic requirement, total analgesic consumption, and block-related adverse effects will be evaluated during the first 24 hours after surgery. The study will assess whether erector spinae plane block provides effective postoperative analgesia comparable to or superior to caudal block in pediatric orchiopexy.


Eligibility

Sex: MALEMin Age: 1 YearMax Age: 7 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a new treatment for people with caudal epidural anesthesia, flacc scale, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include men aged 1 Year to 7 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Prof. Dr Cemil Taşcıoğlu Şehir Hastanesi

Istanbul, şişli, Turkey (Türkiye)

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NCT07762339


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