EOI Block for Laparoscopic Gastrostomy

ConditionGastrostomy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age3-17
SponsorSeoul National University Hospital

About this trial

This randomized controlled trial will evaluate the efficacy of ultrasound-guided external oblique intercostal fascial plane (EOI) block in reducing intraoperative and postoperative pain in pediatric patients undergoing laparoscopic gastrostomy under general anesthesia. Forty patients aged 3-18 years will be randomly allocated to receive either bilateral EOI block with 0.25% ropivacaine or sham block with normal saline. Primary outcome is percent change in heart rate at surgical incision. Secondary outcomes include intraoperative fentanyl use, perioperative analgesic requirements, postoperative pain scores (r-Face, Legs, Activity, Cry, Consolability(r-FLACC) and Pediatric Pain Profile), Analgesia Nociception Index values, and analgesia-related adverse events.

Eligibility criteria

Qualifiers

Scheduled for laparoscopic gastrostomy at Seoul National University Children's Hospital

Disqualifiers

Unstable vital signs

Trial design

Treatments tested in this trial

  • EOI block
  • sham block

Treatment groups

40 Participants
are divided into 2 treatment groups