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Study identifier: NCT07119346 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

EOI Block for Laparoscopic Gastrostomy

Condition: Gastrostomy  ·  Sponsor: Seoul National University Hospital

PhaseNA
Planned participants40
Who can joinAll sexes, 3 Years to 17 Years
Healthy volunteersNo

About this study

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.

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

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Locations (1)

Seoul National University Children's HospitalSeoul, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT07119346