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Clinical Trials in Turkey / NCT07711496
Starting soon Not applicable

Retrolaminar Plane Block Versus Anterior Quadratus Lumborum Block in Pediatric Urogenital Surgery

NCT07711496 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-07-25
Last updated
2026-07-17

Condition(s) studied

Pediatric Regional AnesthesiaRetrolaminar BlockPediatric Postoperative Pain

Investigational drug(s) / intervention(s)

Anterior Quadratus Lumborum BlockRetrolaminar Block

Anterior Quadratus Lumborum Block: An ultrasound-guided anterior quadratus lumborum block will be performed after induction of general anesthesia. Following identification of the quadratus lumborum and psoas major muscles, 0.25 percent bupivacaine will be injected into the fascial plane between these muscles at a volume of 0.4 milliliters per kilogram.

Retrolaminar Block: An ultrasound-guided retrolaminar block will be performed after induction of general anesthesia. After identification of the target vertebral lamina, 0.25 percent bupivacaine will be administered into the retrolaminar plane at a volume of 0.4 milliliters per kilogram.

Study summary

Effective control of postoperative pain following pediatric lower urogenital surgery is important for enhancing recovery and reducing opioid requirements. Anterior quadratus lumborum block and retrolaminar block are two ultrasound-guided truncal block techniques used for perioperative analgesia in lower abdominal surgery. However, direct comparisons of their analgesic efficacy in pediatric lower urogenital procedures remain limited.

This prospective, randomized, controlled trial will enroll 76 pediatric patients aged 6 months to 12 years with American Society of Anesthesiologists physical status I-III who are scheduled for elective lower urogenital surgery. Participants will be randomly assigned in a 1:1 ratio to receive either an anterior quadratus lumborum block or a retrolaminar block. Both techniques will be performed under ultrasound guidance in addition to standardized general anesthesia.

The primary outcome will be rescue analgesic requirement during the first 24 postoperative hours. Secondary outcomes will include postoperative pain scores, time to first rescue analgesic administration, intraoperative remifentanil consumption, adverse effects such as nausea and vomiting, and caregiver satisfaction. The study aims to compare the postoperative analgesic efficacy and safety of anterior quadratus lumborum block and retrolaminar block in pediatric patients undergoing lower urogenital surgery.

Eligibility

Sex
ALL
Min age
6 Months
Max age
12 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 6 months and 12 years * Scheduled for lower abdominal urogenital surgery (e.g., inguinal hernia repair or orchiopexy for undescended testis) * American Society of Anesthesiologists physical status classification I-III * Written informed consent obtained from a parent or legal guardian Exclusion Criteria: * History of allergy to local anesthetic agents * Presence of infection at the planned injection site * Coagulopathy or any other condition contraindicating regional anesthesia * Planned laparoscopic orchiopexy * American Society of Anesthesiologists physical status classification IV * Inability to obtain informed consent from a parent or legal guardian * Anticipated requirement for postoperative intensive care unit admission

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Istanbul University-Cerrahpasa, Cerrahpasa Medicine of Faculty Bakırköy Istanbul

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Other trials for the same condition

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 NCT07711496 on ClinicalTrials.gov ↗ ← All trials in Turkey