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Study identifier: NCT06725862 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Caudal Block vs Retrolaminar Block on Analgesic Consumption in Undescended Testis Surgeries

Condition: Post Operative Pain  ·  Sponsor: Kanuni Sultan Suleyman Training and Research Hospital

PhaseNA
Planned participants60
Who can joinMale, 1 Year to 7 Years
Healthy volunteersNo

About this study

This study compares the postoperative analgesic effectiveness of Caudal Block (CB) and Retrolaminar Block (RLB) in pediatric patients undergoing undescended testis surgeries. Both techniques aim to manage pain effectively and reduce reliance on systemic analgesics, improving recovery and minimizing complications. The double-blind, randomized controlled trial will include 1-7-year-old ASA I-II patients at two hospitals. Patients with specific contraindications (e.g., spinal anomalies, allergies, or infections) will be excluded. Randomization divides participants into two groups (CB and RLB), with pain assessments performed using the FLACC pain scale by a blinded nurse. Procedures: CB: 0.125% bupivacaine (1 mL/kg, max 20 mL) injected into the sacral canal under ultrasound guidance. RLB: 0.25% bupivacaine (0.1 mL/kg) injected into the retrolaminar space at the L4 level under ultrasound guidance. Postoperative pain will be evaluated at various intervals (30 minutes to 24 hours). Intravenous paracetamol or tramadol will be administered based on pain scores. The study aims to compare pain scores, time to first analgesic requirement, and postoperative complications, contributing valuable data on these two regional anesthesia techniques in pediatric surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Engin ihsan Turan  ·  05382431114  ·  enginihsan@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (2)

Health Science University İstanbul Kanuni Sultan Süleyman Education and Training HospitalIstanbul, Turkey (Türkiye)Recruiting
Zincirlikuyu Medicana HospitalIstanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT06725862