Actively Recruiting

Age: 6Months - 16Years
All Genders
Healthy Volunteers
NCT07242196

Transversalis Fascia Plane Versus Transversus Abdominis Plane Block for Postoperative Analgesia in Children

Led by Sakarya University · Updated on 2026-03-10

36

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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 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 this approach, targets the proximal portions of the T12 and L1 nerves by depositing local anesthetic between the transversus abdominis muscle and the transversalis fascia, potentially offering wider sensory coverage. This study compares both blocks in terms of postoperative pain scores, duration of analgesia, and requirement for rescue analgesics in children undergoing laparoscopic surgery. The results are expected to contribute to the optimization of regional anesthesia techniques and improve pain management strategies in pediatric surgical patients.

CONDITIONS

Official Title

Transversalis Fascia Plane Versus Transversus Abdominis Plane Block for Postoperative Analgesia in Children

Who Can Participate

Age: 6Months - 16Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pediatric patients aged 6 months to 16 years
  • Classified as ASA physical status I or II
  • Scheduled to undergo laparoscopic surgery under general anesthesia
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sakarya University-Anesthesiology and Reanimation Department

Sakarya, Serdivan, Turkey (Türkiye), 54050

Actively Recruiting

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Research Team

B

Burçin Medicine Doctor

CONTACT

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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