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Determine if genicular nerve radiofrequency ablation (RFA) is a clinically effective intervention for patients with chronic knee pain post-total knee arthroplasty (TKA) as defined by pain.
More than 600,000 total knee arthroplasty (TKA) surgeries are performed each year in the United States, and approximately 20% of patients will experience some element of chronic knee pain or dissatisfaction related to pain following this procedure. The options for management are limited, and physicians often resort to chronic opioid management. This creates a less than ideal situation for our elderly population who are more sensitive to the deleterious effects of opioids and who would greatly benefit from pain-free, independent mobility. The investigators propose a single-arm pilot study looking at performing fluoroscopically guided genicular nerve radiofrequency ablation (RFA) for patients with chronic (>6 months) knee pain following a TKA.
A new paradigm for treating post-TKA pain may be the use of RFA of the articular sensory nerve supply of the knee capsule, to desensitize the knee by blocking sensory afferents of the anterior capsule and thereby decreasing pain. While this modality has demonstrated efficacy for chronic knee pain due to osteoarthritis (OA) in the native knee, only one underpowered study has investigated this technique in chronic pain post-TKA. Further, this study targeted only three genicular nerves, while newer cadaveric studies have suggested multiple additional sensory nerves which if ablated may result in increased pain relief. A placebo-controlled explanatory trial of genicular nerve RFA for chronic pain post-TKA of appropriate size and statistical methodology has not been conducted.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Total Knee Arthroplasty | Patients who have undergone total knee arthroplasty post one-year. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Genicular Nerve Radiofrequency Ablation | Other | Radiofrequency Ablation (RFA) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Numeric ranking scale (NRS) pain | NRS pain score (0 no pain - 10 severe pain) | Prior to nerve radiofrequency ablation (RFA) |
| Numeric ranking scale (NRS) pain | NRS pain score (0 no pain - 10 severe pain) | 1-month post-genicular nerve RFA |
| Numeric ranking scale (NRS) pain | NRS pain score (0 no pain - 10 severe pain) | 3-months post-genicular nerve RFA |
| Numeric ranking scale (NRS) pain | NRS pain score (0 no pain - 10 severe pain) | 6-months post-genicular nerve RFA |
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Inclusion Criteria:
Exclusion Criteria:
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Patients who have high pain following total knee replacement identified in clinic.
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| Name | Affiliation | Role |
|---|---|---|
| Lucas Anderson, MD | University of Utah Orthopaedics | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Utah Orthopaedic Center | Salt Lake City | Utah | 84108 | United States |
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