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Comparison of PENG Associated with LFCN Block Versus FICB for Multimodal Analgesic Management in THA

O

Ospedale Edoardo Bassini

Status

Completed

Conditions

Hip Arthropathy
Arthropathy of Hip
Regional Anesthesia Morbidity
Anesthesia Complication
Post Operative Pain

Treatments

Procedure: FIC Block
Procedure: PENG plus LFCN block

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Optimal pain control with limited muscle weakness is paramount for a swift initiation of physical therapy and ambulation. Fascia iliaca compartment block (FIC) has been recommended since it offers the best pain control with low risk of motor block. Pericapsular nerve group block (PENG) with lateral femoral cutaneous block (LFCN) has been proposed as an effective alternative to FIB that offers similar pain control with a considerably lower risk of motor block. The aim of this study is to compare the afore mentioned blocks and determine which one yielded the least degree of quadriceps femoris muscle weakness and the better pain control (the lowest NRS score with least need for opioids).

Full description

This single-center, double blinded RCT investigation will be conducted at ASST Nord Milano - Bassini hospital. The study was approved by the ethics committee "Comitato Etico Territoriale Lombardia 3".

Each patient undergoing elective total hip replacement surgery with anterior approach will be subjected (unless contraindicated) to subarachnoid neuraxial anesthesia and immediately afterwards to a peripheral analgesic block: the FIC block or the association of PENG and FCLN block. The choice of block type will be randomized.

At the end of the procedure, a clinician unaware of the anesthetic technique used will assess the degree of residual motor block. Simultaneously, he will assess pain control in terms of NRS (Numerical Rating Scale) and the need for opioid use.

Enrollment

58 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • elective total hip replacement surgery for non-traumatic hip disease,
  • THA (total hip arthroplasty) with lateral approach
  • age >18 years,
  • signed consent form for spinal anesthesia and peripheral nerve block provided by the patient or legal guardian if appointed

Exclusion criteria

  • Non elective THA
  • Lack of consent to the procedure
  • Contraindications to performing neuraxial anesthesia (i.e. Signs suggestive of puncture site infection, INR > 1.5, aPTT > 1.5, PLT < 40.000)
  • Documented or suspected allergy to local anesthetics

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

58 participants in 2 patient groups

PENG - LFCN Block
Experimental group
Description:
group in which PENG and LFCN Block was performed. After performing neuraxial anesthesia, the PENG associated with LFCN block will be performed. Under ultrasound guidance, 20ml and 5ml of Ropivacaine 0.5% will be administered respectively.
Treatment:
Procedure: PENG plus LFCN block
FIC Block
Active Comparator group
Description:
group in which FIC Block was performed After performing neuraxial anesthesia, FIC block will be performed. Under ultrasound guidance, 20 ml of Ropivacaine 0.5% will be administered.
Treatment:
Procedure: FIC Block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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