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

Ultrasound-Guided Transversalis Fascia Plane Block Versus Caudal Block for Postoperative Analgesia in Children Undergoing Inguinal Herniorrhaphy: A Randomized Controlled Non-Inferiority Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06725667
Enrollment
50
Registered
2024-12-10
Start date
2024-12-11
Completion date
2025-12-06
Last updated
2025-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief summary

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.

Detailed 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

Interventions

Patients will receive transversalis fascia plane block after the induction of general anesthesia.

OTHERCaudal block

Patients will receive caudal block after the induction of general anesthesia.

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Years to 7 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Time to the 1st rescue analgesia24 hours postoperativelyTime to the first request for the rescue analgesia (time from the end of surgery to first dose of paracetamol administrated).

Secondary

MeasureTime frameDescription
Intraoperative fentanyl consumptionIntraoperativelyAdditional fentanyl bolus dosages of 1 µg/kg IV will be administered if heart rate or mean arterial blood pressure elevated more than 20% of the baseline (after exclusion of other causes than pain).
Degree of pain24 hours postoperativelyDegree of pain will be assessed using the Face, legs, activity, cry, and consolability (FLACC) scale. Each of the five items of the FLACC scale will be scared, ranging from 0 to 2, which will be then aggregated to obtain a total score ranging from 0 to 10. Higher scores on the scale indicated a higher level of pain intensity.
Hear rateEvery 15 min till the end of surgery (Up to 2 hours)Hear rate will be recorded preoperatively, before performing of block, and every 15 min till the end of surgery.
Total paracetamol consumption24 hours postoperativelyEach of the five items of the Face, legs, activity, cry, and consolability (FLACC) scale will be scared, ranging from 0 to 2, which will be then aggregated to obtain a total score ranging from 0 to 10. Higher scores on the scale indicated a higher level of pain intensity. If the FLACC scale exceeds three, IV paracetamol (15 mg/kg) will be given.
Degree of patient's parents satisfaction24 hours postoperativelyDegree of patient's parents satisfaction will be assessed on a 5-point Likert scale patient satisfaction (1, extremely dissatisfied; 2, unsatisfied; 3, neutral; 4, satisfied; 5, extremely satisfied)
Incidence of adverse events24 hours postoperativelyIncidence of adverse events such as bradycardia, hypotension, nausea, vomiting, respiratory depression, or any other complication related to block such as hematoma, neurological injury, deep visceral injury, or local anesthetic toxicity will be recorded.
Mean arterial pressureEvery 15 min till the end of surgery (Up to 2 hours)Mean arterial pressure will be recorded preoperatively, before performing of block, and every 15 min till the end of surgery.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026