Sacral Erector Spinae Plane Block Versus Penile Block For Analgesia In Pediatric Circumcision

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-12
SponsorIstanbul University - Cerrahpasa

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)

Treatment groups

60 Participants
are divided into 2 treatment groups