About this trial
Circumcision is one of the most frequently performed surgical procedures in childhood and is associated with significant postoperative pain. This randomized controlled trial (RCT) aims to compare the analgesic effectiveness of sacral erector spinae plane block (sacral ESPB) and penile nerve block (PNB) in children undergoing circumcision surgery. The primary outcome is postoperative pain, assessed using the Face, Legs, Activity, Cry, and Consolability (FLACC) scale at predefined time intervals within the first 24 hours after surgery. Secondary outcomes include intraoperative analgesic consumption, time to first postoperative analgesic requirement, perioperative hemodynamic changes. The results of this study are expected to provide evidence for selecting the optimal regional analgesic technique for pediatric circumcision surgery.
Eligibility criteria
Qualifiers
Age between 1 and 12 years
Scheduled for circumcision surgery
Classified as American Society of Anesthesiologists (ASA) physical status I-II
Written informed consent obtained from both the participant (when appropriate) and their parents or legal guardians
Disqualifiers
Age under 1 year or over 12 years
Undergoing circumcision combined with other surgical procedures
Presence of neurological deficits
History of bleeding diathesis
Trial design
Treatments tested in this trial
- Sacral Erector Spinae Plane Block
- Penile Nerve Block (PNB)