Comparison of the Analgesic Efficacy of Transversalis Fascia Plane Block and Posterior Quadratus … (NCT07286799) | Clinical Trial Compass
CompletedNot Applicable
Comparison of the Analgesic Efficacy of Transversalis Fascia Plane Block and Posterior Quadratus Lumborum Block in Pediatric Patient Undergoing Orchiopexy: A Prospective Observational Study
It was planned to compare the analgesic efficacy of the transversalis fascia plane block and the posterior quadratus lumborum block in children aged 1 to 7 years undergoing orchiopexy, by evaluating their FLACC scores and the time to first postoperative analgesic requirement.
Who can participate
Age range1 Year – 7 Years
SexMALE
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Inclusion Criteria:
* Children aged 1 to 7 years with ASA physical status I-II undergoing unilateral orchiopexy surgery.
Exclusion Criteria:
* ASA physical status ≥ III
* History of prematurity (gestational age \< 37 weeks) Known coagulation disorders or bleeding tendency
* Infection, inflammation, or skin lesion at the injection site
* Known neurological or neuromuscular diseases
* Presence of significant cardiac or pulmonary disease (e.g., congenital heart disease, active asthma)
* Hepatic or renal dysfunction
* Known allergy or hypersensitivity to local anesthetics (e.g., bupivacaine, lidocaine)
* Developmental delay or cognitive impairment that prevents accurate pain assessment
* Use of additional regional analgesia techniques (e.g., caudal block) during surgery
* Block failure or intraoperative complications requiring exclusion from protocol analysis
* Lack of parental consent for participation in the study
What they're measuring
1
Time to First Analgesic Requirement After Surgery
Timeframe: First 24 hours postoperatively
Trial details
NCT IDNCT07286799
SponsorProf. Dr. Cemil Tascıoglu Education and Research Hospital Organization