External Oblique Intercostal Plane Block vs Erector Spinae Plane Block for Paediatric Upper Abdominal Surgeries
Official title: Ultrasound Guided External Oblique Intercostal Plane Block Versus Erector Spinae Plane Block in Paediatric Upper Abdominal Surgeries
Run by Alexandria University · NCT07617545 · Data updated 2026-11-12
This study tests whether two ultrasound-guided nerve blocks—external oblique intercostal plane and erector spinae plane—provide different pain relief for children undergoing upper abdominal surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 6 Years to 12 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Alexandria University Academic / other |
| Locations | 1 site (Alexandria) |
| Status | Recruiting |
| Started | May 1, 2025 |
| Main results expected | October 1, 2026 |
| Study ends | October 1, 2026 |
| Registry record updated | June 1, 2026 |
| Trial ID | NCT07617545 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Children aged 6 to 12 years with ASA I–II status undergoing upper abdominal surgery and without contraindications to regional anesthesia.
✕Probably not a fit
Children who do not respond to regional anesthesia or who have contraindications to local anesthetics or block complications may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study compares two ultrasound-guided regional anesthesia techniques in pediatric patients aged 6 to 12 years undergoing upper abdominal surgery. The goal is to determine which block offers better postoperative pain control and recovery with minimal side effects. Blocks target pain pathways differently: the external oblique intercostal plane block anesthetizes thoracoabdominal nerves, while the erector spinae plane block delivers anesthetic in a fascial plane near the spine. Outcomes likely include pain scores, opioid use, recovery metrics, and safety events. Eligibility includes ASA I/II children without contraindications and within a surgery duration window.
Why it matters
Potential benefit: If successful, one block may provide superior pain relief with faster recovery and less opioid need in pediatric upper abdominal surgery.
How similar studies have gone: Prior pediatric regional anesthesia studies show promising pain control with nerve blocks, but direct comparison of these two techniques is novel in this setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Children aged between 6 and 12 years of both sex. * Patients with the American Society of Anesthesiologists (ASA) physical status I/II. * Patients undergoing upper abdominal surgeries involving upper abdominal incisions. Exclusion Criteria: * Guardian refusal. * Allergy to local anesthetics. * Surgical procedures exceeding 3 hours. * Infection at the area planned for the block injection. * Prolonged opioid medication. * Patients preoperatively medicated by Beta blockers
Where it's running
-
Alexandria University
Alexandria, Egypt Recruiting
Study contacts
- Study coordinator: Belal M Hassan, MBBCH
- Email: Belal.bakr1420@alexmed.edu.eg
- Phone: 00201091397908
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.