Pericapsular Nerve Group Block Chemical Neurolysis in Advanced Hip Osteoarthritis

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-17

Study Completion Date

2025-01-14

Brief Summary

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PENG neurolysis in advanced osteoarthritis of the hip joint.

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Detailed Description

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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.

Conditions

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Osteoarthritis Osteoarthritis, Hip

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Group 1 - PENG sham block Group 2 - PENG neurolysis 95% ethanol

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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sham PENG block

PENG block - 20ml 0,9% normal saline

Group Type ACTIVE_COMPARATOR

0.9%sodium chloride

Intervention Type DRUG

PENG sham block with 20ml 0,9% normal saline

PENG neurolysis

PENG neurolysis with 5ml 95% ethanol

Group Type ACTIVE_COMPARATOR

95% ethanol

Intervention Type DRUG

PENG neurolysis with 2.5ml of 95% ethanol

Interventions

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0.9%sodium chloride

PENG sham block with 20ml 0,9% normal saline

Intervention Type DRUG

95% ethanol

PENG neurolysis with 2.5ml of 95% ethanol

Intervention Type DRUG

Other Intervention Names

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Sham block neurolysis

Eligibility Criteria

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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.