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Pericapsular Nerve Group Block Chemical Neurolysis in Advanced Hip Osteoarthritis (PENG)

P

Poznan University of Medical Sciences (PUMS)

Status and phase

Completed
Phase 4

Conditions

Osteoarthritis, Hip
Osteoarthritis

Treatments

Drug: 0.9%sodium chloride
Drug: 95% ethanol

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

PENG neurolysis in advanced osteoarthritis of the hip joint.

Full description

The study aims to assess the safety and effectiveness of regional pain treatment methods and their impact on the quality of life of patients with advanced osteoarthritis of the hip joint.

Enrollment

100 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients of the Pain Treatment Clinic of the Transfiguration of Jesus Clinical Hospital of the Medical University of Poznań will be qualified for the study
  • patients with coxarthrosis or gonarthrosis who failed to achieve satisfactory pain control (NRS>3) despite the use of NSAIDs, Paracetamol, and co-analgetics
  • Age of patients: from 18 to 110 years of age.
  • Caucasian patients can give informed, complete, written consent.

Exclusion criteria

  • suspected or diagnosed opioid dependence syndrome
  • active cancer
  • dementia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

100 participants in 2 patient groups

sham PENG block
Active Comparator group
Description:
PENG block - 20ml 0,9% normal saline
Treatment:
Drug: 0.9%sodium chloride
PENG neurolysis
Active Comparator group
Description:
PENG neurolysis with 5ml 95% ethanol
Treatment:
Drug: 95% ethanol

Trial contacts and locations

1

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Central trial contact

Malgorzata Domagalska, Ph.D.

Data sourced from clinicaltrials.gov

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