Radiofrequency Ablation on Pain Relief of Knee Osteoarthritis
Osteoarthritis, Knee
About this trial
This is an interventional treatment trial for Osteoarthritis, Knee
Eligibility Criteria
Inclusion Criteria:
- Patients with intractable knee pain intensity >5 on an 11-point visual analog scale (VAS) (where 0=no pain and 10=worst pain imaginable) for longer than three months and unable to do knee replacement surgery.
- Age > 50 years.
- Grade 2 or 3 KOA based on the Kellgren-Lawrence classification.
- Patients who did not respond to conservative treatment (physiotherapy, oral NSAIDs, and/or intraarticular injections of hyaluronic acid and corticosteroid) for 3 months.
- Duration of knee pain ≥ 3 months.
- Numeric rating scale (NRS) ≥ 5 points within 24 h prior to admission.
Exclusion Criteria:
- Grade 1 or 4 KOA based on the Kellgren-Lawrence classification.
- Severe liver, kidney, cardiovascular, and respiratory disease.
- Abnormal blood coagulation.
- Skin infections in the puncture region.
- Patients who previously underwent knee arthroscopy, TKA, RFTGN, or IAPRF.
- Mental disorders or inability to complete the follow-up observational form.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Cooled radio frequency
Thermocoagulant radio frequency
In CRF, water circulates inside the probe to remove heat, modulating the thermal heat in the tissue to around 60°C, and alters the overall size, shape, and projections of lesions compared to conventional RFA. It is postulated that the greater sized CRF lesions may reduce the number of technical failures in the setting of a complex and variable neuronal innervation to the knee. The ability to target a greater amount of neuronal tissue is believed to produce long-term pain relief at least to the duration of relief produced by conventional RFA [27]
Conventional radiofrequency Ablation RFA of the knee can be performed under fluoroscopic, or other imaging, guidance, with a cannula advanced into the joint towards the area connecting the shaft to the epicondyle. The area is stimulated to identify the nerve position and to ensure that no motor nerves are activated, as evidenced by absence of fasciculations. The RF electrode is then advanced through the cannula to the target area [18] The electrode tip heats up targeted local tissue within a few millimeters to a temperature typically greater than 47°C (ranging from 70°C to 90°C) for 120 130 seconds, generated through an electromagnetic field with a frequency of 250 kHz . [15,18] The ablative heat is provided via flow of electrical current, generating a well-delineated lesion [24]