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Clinical Trials in Egypt / NCT07666334
Recruiting Not applicable

Subtransverse Process Interligamentary Plane Block Versus Rhomboid Intercostal Block Combined With Sub-Serratus Plane Block for Analgesia in Pediatric Thoracotomy

NCT07666334 · tracked via the Priya Life Science Egypt tracker
Sponsor
Tanta University
Phase
Not applicable
Started
2025-09-01
Last updated
2026-06-24

Condition(s) studied

Subtransverse Process Interligamentary Plane BlockRhomboid Intercostal BlockSub-Serratus Plane BlockAnalgesiaPediatric Thoracotomy

Investigational drug(s) / intervention(s)

Standard intravenous analgesiaSubtransverse process interligamentary plane blockRhomboid intercostal block (RIB) combined with sub-serratus plan block group

Standard intravenous analgesia: Patients will receive no block intervention and standard intravenous analgesia will be given.

Subtransverse process interligamentary plane block: Patients will receive ipsilateral ultrasound-guided subtransverse process interligamentary (STIL) plane block with bupivacaine 0.25% (0.5 mL/kg) after induction of general anesthesia.

Rhomboid intercostal block (RIB) combined with sub-serratus plan block group: Patients will receive ipsilateral ultrasound-guided rhomboid intercostal block (RIB) combined with sub-serratus plan block group with bupivacaine 0.25% (0.5mL/kg) after induction of general anesthesia.

Study summary

This study aims to compare ultrasound guided subtransverse process interligamentary plane block versus rhomboid intercostal block combined with sub-serratus plane block for postoperative analgesia in pediatric thoracotomy.

Eligibility

Sex
ALL
Min age
6 Years
Max age
12 Years
Healthy volunteers
No
Inclusion Criteria: * Pediatric patients between 6 to 12 years. * Both sexes. * American Society of Anesthesiologists (ASA) Physical Status I - II. * Scheduled for thoracic surgery with thoracotomy incision under general anesthesia. Exclusion Criteria: * Parents who refused regional anesthesia. * Patients were presented with advanced kidney, cardiac or liver diseases. * Coagulation and bleeding disorders. * Patients presented with skin or soft tissue infection at the proposed site of needle Insertion. * Patients with cognitive impairment.

Primary outcome measure(s)

  • Time to first rescue analgesia — 24 hours postoperatively
    Time to the first rescue analgesia will be recorded from the end of surgery till first dose of morphine adminstrated.

Trial sites (1)

FacilityCityRegionStatus
Tanta University Tanta El-Gharbia Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07666334 on ClinicalTrials.gov ↗ ← All trials in Egypt