Phenol Neurolysis of Genicular Nerves for Osteoarthritic Knee Pain

Kessler Foundation

Status and phase: Unknown; Phase 4

Conditions: Knee Pain Chronic; Osteoarthritis, Knee

Treatments: Drug: Isotonic saline; Drug: 6% aqueous phenol

Study type: Interventional

Funder types: Other

Identifiers

NCT04989660

R-1154-21

Details and patient eligibility

About

As the aging and obese populations continue to increase, there is a rapidly growing number of people at risk for knee osteoarthritis. Treatment typically starts conservatively with analgesics, physical therapy, and bracing. Intra-articular injections with corticosteroids and/or viscosupplementation may also be utilized in those with persistent knee pain. Genicular nerve radiofrequency ablation (GNRFA) is an increasingly employed procedure for refractory osteoarthritic knee pain with promising efficacy for pain relief. However, due to its reliance on expensive equipment, additional staff, and need for specialized rooms (eg. fluoroscopy suite), GNRFA is a costly procedure with limited availability. Chemical neurolysis is an alternative method of nerve ablation using alcohol or phenol utilized in the management of pain. Recent literature has demonstrated good efficacy for pain relief and function with chemical ablation of the genicular nerves using both alcohol and phenol.

This study is a double-blind, randomized, placebo-controlled pilot study to assess the efficacy of phenol neurolysis of the genicular nerves for pain and function due to refractory osteoarthritic knee pain. We hypothesize that a significant improvement in both pain and function will be observed with chemical neurolysis of the genicular nerves using 6% phenol compared to placebo.

Enrollment: 30 estimated patients

Sex: All

Ages: 40+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Radiographic knee osteoarthritis (Kellgren-Lawrence grade 2-4)
• Knee pain of moderate intensity or greater (NRS of 4 or greater)
• Knee pain for 3 months or longer
• Persistent knee pain despite conservative treatment including oral/topical analgesics, physiotherapy, intra-articular injection with corticosteroid and/or hyaluronic acid

Exclusion criteria

• Prior total or partial knee arthroplasty in the knee(s) to be treated
• Prior radiofrequency ablation treatment in the affected knee
• Other rheumatological or connective tissue disease(s) affecting the knee to be treated
• History of bleeding disorder
• Any psychiatric or neurologic disease (eg. dementia, brain injury, etc.) that may preclude reliable reporting of symptoms and response to treatment
• Pregnancy
• Recent treatment with intraarticular hyaluronic acid, platelet-rich plasma, or corticosteroid injections to the affected knee in the past 3 months
• Skin or joint infection in the knee(s) to be treated
• Concomitant radicular pain

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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30 participants in 2 patient groups, including a placebo group

Treatment Group

Experimental group

Description:

6% aqueous phenol, 1.5 mL per target site

Treatment:

Drug: 6% aqueous phenol

Placebo Group

Placebo Comparator group

Description:

Isotonic saline, 1.5 mL per target site

Treatment:

Drug: Isotonic saline