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Transversalis Fascia Plane Versus Transversus Abdominis Plane Block for Postoperative Anal

This prospective clinical study aims to compare the postoperative analgesic efficacy of the ultrasound-guided transversalis fascia plane block (TFPB) and the transversus abdominis plane (TAP) block in pediatric patients undergoing laparoscopic surgery. Effective and long-lasting postoperative analgesia is essential for

Condition(s)Postoperative Analgesia, Transversus Abdominis Plane (TAP) Block, Transversalis Fascia Plane Block, Pediatric Surgical Procedures, Laparoscopic Abdominal Surgeries
StatusRecruiting
Study typeObservational
SummaryThis prospective clinical study aims to compare the postoperative analgesic efficacy of the ultrasound-guided transversalis fascia plane block (TFPB) and the transversus abdominis plane (TAP) block in pediatric patients undergoing laparoscopic surgery. Effective and long-lasting postoperative analgesia is essential for patient and parental satisfaction in pediatric anesthesia. With recent advances in ultrasound technology, regional anesthesia techniques have become increasingly utilized in pediatric practice. In the TAP block, local anesthetic is injected between the internal oblique and transversus abdominis muscles, providing analgesia typically between Torachal vertebra 10 (T10) and Lumbar vertebra (L1) dermatomes. The transversalis fascia plane block, developed as a modification of thi
Who can participateInclusion Criteria: * Pediatric patients aged 6 months to 16 years * Classified as ASA physical status I or II * Scheduled to undergo laparoscopic surgery under general anesthesia Exclusion Criteria: * Patients classified as ASA physical status III or IV * Known allergy or hypersensitivity to local anesthetic agents * Presence of bleeding diathesis or coagulation disorders * Infection at the injection site or local skin lesions preventing block application
Ages6 Months to 16 Years
SexAll
Accepts healthy volunteersYes
Lead sponsorSakarya University
LocationsSakarya, Serdivan, Turkey (Türkiye)
Start date2025-12-18
NCT IDNCT07242196
Official listinghttps://clinicaltrials.gov/study/NCT07242196

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