Ultrasound-Guided Pudendal vs Dorsal Penile Nerve Block for Pediatric Hypospadias Surgery

The goal of this clinical trial is to compare the effectiveness and safety of two regional anesthesia techniques, ultrasound-guided pudendal nerve block and dorsal penile nerve block, for postoperative pain management in children undergoing hypospadias surgery. The main questions we aim to answer are: Which technique provides more effective pain relief after surgery? What are the potential side effects or complications associated with each technique? Participants will: Receive either an Ultrasound-guided pudendal nerve block or a dorsal penile nerve block in combination with general anesthesia after surgery. Participants will be monitored for pain levels using a pediatric pain scale Face, Leg, Activity, Cry, Consolability (FLACC) and their overall recovery for the first 24 hours post-surgery. Have their total analgesic consumption and vital signs recorded during the recovery period. This study will help improve postoperative pain management strategies for pediatric hypospadias surgery by evaluating these two anesthesia techniques.

NCT Number	NCT07575204
Lead Sponsor	Bangladesh Medical University
Conditions	Hypospadias, Pudendal Nerve Block, Penile Nerve Block, Postoperative Pain
Enrollment	60 participants
Start Date	2025-05-01
Primary Completion	2026-03-31 (estimated)
Study Completion	2026-03-31 (estimated)
Updated on ClinicalTrials.gov	2026-05-12