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

NCT07762339 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 84

Last updated 2026-08-13

No results posted yet for this study

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.

Conditions

  • Caudal Epidural Anesthesia
  • Sacral Erector Spinae Plane Block
  • Orchiopexy
  • FLACC Scale

Sponsors & Collaborators

  • Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

    lead OTHER

Principal Investigators

  • kübra demir · Prof. Dr Cemil Taşcıoğlu Şehir Hastanesi

Eligibility

Min Age
1 Year
Max Age
7 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-06-08
Primary Completion
2027-01-08
Completion
2027-01-08

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07762339 on ClinicalTrials.gov