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Pericapsular Nerve Group Block Versus Fascia Iliaca Block for Pediatric Hip Surgery

Not Applicable
Conditions
Pericapsular Nerve
Fascia Iliaca
Hip Surgery
Interventions
Procedure: Caudal Block group
Procedure: Fascia iliaca group
Procedure: Pericapsular nerve group block
Registration Number
NCT05460442
Lead Sponsor
Tanta University
Brief Summary

This compares the postoperative analgesic effect of ultrasound-guided pericapsular nerve group block (PENG) with ultrasound-guided fascia iliaca compartment block in pediatric patients undergoing hip surgery.

Detailed Description

Surgeries involving hip joints in pediatric patients are associated with severe intraoperative and postoperative pain despite the use of systemic opioids.

Caudal block is the most commonly used method of regional anesthesia in children to control intraoperative and postoperative pain in surgeries involving lower limbs. However, there have been many side effects of caudal block such as hypotension, urine retention, excessive motor block, technical failure, nausea, and vomiting which may limit its use.

There are several techniques of ultrasound-guided regional anesthesia that are used to control acute pain in hip surgery with fewer side effects such as a lumbar plexus block, femoral nerve block, or a fascia iliaca compartment block.

The fascia iliaca compartment block (FICB) was described in 1989. It remains a popular regional anesthetic technique for surgical procedures involving the hip joint and femur. Local anesthetic (LA) is injected proximally beneath the fascia iliaca to block the femoral nerve (FN), obturator nerve (ON), and lateral cutaneous nerve of the thigh (LCNT) simultaneously.

The pericapsular nerve group (PENG) block was introduced to block the articular branches of the femoral, obturator, and accessory obturator nerves which provide sensory innervation to the hip. This regional anesthetic technique was described in 2018 for acute analgesia related to hip fractures.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
75
Inclusion Criteria
  • Pediatric patients
  • aged 1-6 years old
  • both sexes,
  • American Society of Anesthesiologists (ASA) physical activity class I-II
  • scheduled for elective hip surgery under general anesthesia.
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Exclusion Criteria
  • Children with the severe systemic disease with American Society of Anesthesiologists physical activity class III or IV.
  • Children with previous neurological or spinal disorders.
  • Coagulation disorder.
  • Infection at the block injection site.
  • History of allergy to local anesthetics.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Caudal Block groupCaudal Block group25 patients will receive ultrasound-guided caudal block with bupivacaine 0.25% (0.5 mL/kg) after induction of anesthesia.
Fascia iliaca groupFascia iliaca group25 patients will receive ipsilateral ultrasound-guided Fascia iliaca compartment block with bupivacaine 0.25% (0.5 m. L/kg) after induction of anesthesia.
Pericapsular nerve group blockPericapsular nerve group block25 patients will receive ipsilateral ultrasound-guided Pericapsular nerve group block with bupivacaine 0.25% (0.5 mL/kg) after induction of anesthesia.
Primary Outcome Measures
NameTimeMethod
Total Opioids consumption24 hours postoperatively

Total Opioids consumption in first 24 hour postoperatively will be recorded

Secondary Outcome Measures
NameTimeMethod
Adverse effects24 hours Postoperatively

Adverse effects: hypotension, Bradycardia, hematoma, and local anesthetic toxicity will be observed and treated accordingly.

Heart rateIntraoperative then at post anesthesia care unit then after 30 minutes 2, 4, 6, 12, 24 hours

Perioperative heart rate will be observed

Postoperative painAt post anesthesia care unit then after 30 minutes 2, 4, 6, 12, 24 hours.

Postoperative pain which will be assessed by face, legs, activity, and cry consolability scale \[FLACC\]

Time to first rescue analgesia24 hours Postoperatively

Time of administration of first rescue analgesia will be recorded.

Mean arterial blood pressureIntraoperative then at post anesthesia care unit then after 30 minutes 2, 4, 6, 12, 24 hours.

Perioperative mean arterial blood pressure will be observed

Trial Locations

Locations (1)

Tanta University hospitals

🇪🇬

Tanta, Egypt

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