Comparing Ultrasound-Guided Transversalis Fascia Plane and Transversus Abdominis Plane Blocks for Pain Relief in Children Undergoing Laparoscopic Surgery
Led by Sakarya University · Updated on 2026-07-07
36
Participants Needed
1
Research Sites
16 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are comparing two types of ultrasound-guided nerve blocks, the transversalis fascia plane block TFPB and the transversus abdominis plane TAP block, to see which provides better pain relief after laparoscopic surgery in children. This study focuses on pediatric patients aged 6 months to 16 years and aims to improve postoperative pain management using regional anesthesia techniques guided by advances in ultrasound technology.
The study involves two groups one receiving the TFPB, where local anesthetic is injected between the transversus abdominis muscle and the transversalis fascia targeting nerves at T12 and L1, and the other receiving the TAP block, where anesthetic is injected between the internal oblique and transversus abdominis muscles targeting the T10 to L1 dermatomes. Both blocks are given before surgery under ultrasound guidance to provide pain relief after the operation.
Participants will have their pain assessed at 1, 2, 4, 8, 12, and 24 hours after surgery using the Visual Analog Scale. Researchers will also monitor the duration of pain relief, the need for additional rescue analgesics, any block-related complications, and both patient and parental satisfaction within 24 hours after surgery. This comprehensive monitoring aims to determine which block offers more effective and longer-lasting postoperative analgesia for children undergoing laparoscopic procedures.
CONDITIONS
Brief Title
Transversalis Fascia Plane Versus Transversus Abdominis Plane Block for Postoperative Analgesia in Children
Research Team
B
Burçin Medicine Doctor
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Scheduled to undergo laparoscopic surgery under general anesthesia
You will not qualify if you...
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
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Treatment
Duration - Single day (surgery day)
Participants receive one of two ultrasound-guided nerve blocks before laparoscopic surgery: the transversalis fascia plane block or the transversus abdominis plane block.
1 visit (ultrasound-guided nerve block and surgery)
Postoperative Monitoring
Duration - 24 hours after surgery
Participants are monitored for pain using the Visual Analog Scale at 1, 2, 4, 8, 12, and 24 hours after surgery. Additional pain medication needs, block-related complications, and patient and parent satisfaction are also recorded.
Multiple assessments during hospital stay
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Published Research Related To This Trial
Improved analgesia with the ilioinguinal block compared to the transversus abdominis plane block after pediatric inguinal surgery: a prospective randomized trial.
Michael J Fredrickson, Clinton Paine, James Hamill