Percutaneous vs Conventional Radiofrequency Applications for the Treatment of Knee Osteoarthritic Pain

Tanta University

Status: Completed

Conditions: Percutaneous; Radiofrequency; Pain; Knee Osteoarthritis; Conventional

Treatments: Device: Percutaneous radiofrequency; Device: Conventional radiofrequency

Study type: Interventional

Funder types: Other

Identifiers

NCT06520371

36264PR670/4/24

Details and patient eligibility

About

This study aims to compare percutaneous and conventional radiofrequency applications for the treatment of knee osteoarthritic pain.

Full description

Osteoarthritis (OA) is a progressive degenerative joint disease that affects the joint cartilage and surrounding tissues. It mostly affects the weight-bearing joints, and in this respect, the knee joint is one of the joints that is most affected.

Radiofrequency (RF) treatment has been used for several painful conditions such as trigeminal neuralgia, cancer pain, and spinal pain. To destroy nerves or disrupt the transmission of pain signals, originally using producing heat lesions, RF current is applied to the trigeminal ganglion, the spinothalamic tracts of the spinal cord, the medial branches of posterior rami, and the dorsal root ganglion. In addition to these, there have been a few attempts to apply RF current for the treatment of painful conditions of joints of the extremities.

Percutaneous radiofrequency ablation (RFA) of articular sensory nerves has recently emerged as an attractive and minimally invasive approach to treat chronic pain due to large-joint osteoarthritis in select patients.

Enrollment: 50 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age > 18 years old.
• Both sexes.
• Patients with knee osteoarthritis.
• Previous conservative treatments longer than 3 months.
• Visual analog scale (VAS)≥ 4.
• Radiological osteoarthritis grades 3 and 4 according to the Kellgren-Lawrence grading system (0 = none, 1 = doubtful, 2 = minimal, 3 = moderate, and 4 = severe).

Exclusion criteria

• Prior knee surgery.
• Allergies to local anesthetics.
• Connective tissue diseases affect the knee.
• Serious neurologic or psychiatric disorders.
• Injection with steroids or hyaluronic acids during the previous 3 months.
• History of septic arthritis.
• Sciatic pain.
• Cardiac pacemaker users.
• Anticoagulant medications.
• Prior electroacupuncture treatment.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

Percutaneous radiofrequency group

Experimental group

Description:

Patients will receive percutaneous radiofrequency.

Treatment:

Device: Percutaneous radiofrequency

Conventional radiofrequency group

Active Comparator group

Description:

Patients will receive conventional radiofrequency.

Treatment:

Device: Conventional radiofrequency