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Ultrasound-Guided Transversalis Fascia Plane Block Versus Caudal Block for Postoperative Analgesia in Children Undergoing Inguinal Herniorrhaphy

T

Tanta University

Status

Completed

Conditions

Postoperative Analgesia
Caudal Block
Transversalis Fascia Plane Block
Children
Inguinal Herniorrhaphy
Ultrasound

Treatments

Other: Transversalis fascia plane block
Other: Caudal block

Study type

Interventional

Funder types

Other

Identifiers

NCT06725667
36264PR935/11/24

Details and patient eligibility

About

The aim of this study is to compare ultrasound-guided transversalis fascia plane block and caudal block for postoperative analgesia in children undergoing inguinal herniorrhaphy.

Full description

Surgical repair of inguinal hernia is one of the most common day-case surgeries in the pediatric population. It is associated with significant postoperative pain and discomfort.

Caudal block analgesia is a popular and reliable technique for lower abdominal surgeries and found to be safe and effective for providing intra and postoperative analgesia in pediatric patients.

transversal fascia plane block (TFPB) aims to provide analgesia for invasive procedures of the inguinal and sublingual areas by blocking the subcostal (T12), ilioinguinal (L1) and iliohypogastric (T12-L1) nerves. Several studies have reported TFPB as the analgesic method of choice for procedures involving the T12-L1 dermatome region, including iliac bone graft harvesting, cesarean section, and inguinal hernia repair

Enrollment

50 patients

Sex

All

Ages

1 to 7 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age from 1 to 7 years.
  • Both sexes.
  • American Society of Anesthesiology (ASA) physical status I-II.
  • Scheduled for inguinal herniorrhaphy under general anesthesia (GA).

Exclusion criteria

  • Repeated surgeries.
  • Known allergic reactions to any of the study's drugs.
  • Infection at the site of block needle entry.
  • Bleeding diathesis.
  • Neurological disorders.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Transversalis fascia plane block group
Experimental group
Description:
Patients will receive transversalis fascia plane block after the induction of general anesthesia.
Treatment:
Other: Transversalis fascia plane block
Caudal block group
Active Comparator group
Description:
Patients will receive caudal block after the induction of general anesthesia.
Treatment:
Other: Caudal block

Trial contacts and locations

1

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Central trial contact

Mohammed S Elsharkawy, MD

Data sourced from clinicaltrials.gov

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