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PENG Block in Comparison With FICB for Hip Reconstruction in Children

S

Saint Petersburg State University, Russia

Status

Enrolling

Conditions

Perioperative Analgesia
Hip Dislocation, Developmental

Treatments

Procedure: Pericapcelar group nerve block
Procedure: Fascia iliaca compartment block

Study type

Interventional

Funder types

Other

Identifiers

NCT06210503
PENG vs FICB

Details and patient eligibility

About

The goal of this clinical trial is to test the hypothesis that performing a Pericapsular nerve group (PENG) block allows for more effective analgesia in the perioperative period during reconstructive surgery on the hip in children with cerebral palsy and spina bifida compared with Fascia illiaca compartment block (FICB).

Full description

The main question it aims to answer is: Is the PENG block an effective and safe method of pain relief for hip surgery in children? Participants will be randomized into two equal groups. The group who underwent US - guided PENG block, and the group who underwent US - guided FICB . In both groups we used 0.5% ropivacaine. The same postoperative analgesia regimen was applied by intravenous acetaminophen , oral ibuprofen . In case of ineffectiveness of the prescribed drugs, promedol was used intramuscularly. The postoperative consumption of promedol, time to first rescue analgesia, numerical pain score (NRS) (for children from 7 years old), FLACC score, measurements of A.N.I. monitor MDMS and the side effects will be recorded

Enrollment

86 estimated patients

Sex

All

Ages

3 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • reconstructive surgery on the hip joint
  • children with cerebral palsy
  • children with spina bifida
  • age 3 - 18 years.

Exclusion criteria

  • contraindications to the use of local anesthetics
  • contraindications to performing an invasive procedure
  • ASA > 3

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

86 participants in 2 patient groups

PENG group
Active Comparator group
Description:
The patient will undergo pericapsular nerve blockade with 0.5% ropivacaine based on 3 mg/kg ropivacaine using ultrasound scanning.
Treatment:
Procedure: Pericapcelar group nerve block
FICB group
Active Comparator group
Description:
The patient will undergo FICB with 0.5% ropivacaine based on 3 mg/kg ropivacaine using ultrasound scanning.
Treatment:
Procedure: Fascia iliaca compartment block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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