Non-invasive treatment for knee osteoarthritis using pulsed radiofrequency acupuncture
The Efficacy of Transcutaneous Pulsed Radiofrequency Acupuncture for Knee Osteoarthritis
This study is testing a new, non-invasive acupuncture treatment combined with rehab to see if it can help people aged 45 to 85 with knee osteoarthritis feel less pain and get more active.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 45 Years to 85 Years |
| Sex | All |
| Sponsor | Shin Kong Wu Ho-Su Memorial Hospital Academic / other |
| Locations | 1 site (Taipei, State) |
| Trial ID | NCT06702046 on ClinicalTrials.gov |
What this trial studies
This study evaluates the efficacy of transcutaneous pulsed radiofrequency acupuncture combined with rehabilitation for patients suffering from knee osteoarthritis. It targets individuals aged 45 to 85 who experience chronic knee pain and meet specific clinical criteria for osteoarthritis. The approach aims to provide effective pain relief without the invasiveness of traditional acupuncture, thereby encouraging greater participation in rehabilitation activities. Participants will undergo a treatment regimen over four weeks, followed by a three-month follow-up period to assess outcomes.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 45 to 85 with chronic knee pain and a diagnosis of knee osteoarthritis.
Not a fit: Patients with infections, autoimmune diseases, or those who have undergone knee surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve pain management and functional outcomes for patients with knee osteoarthritis.
How similar studies have performed: Previous studies have shown positive outcomes with traditional acupuncture and electroacupuncture for knee osteoarthritis, suggesting potential for success with this novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 45 to 85 year-old with knee pain for more than six months * Fulfill the combined clinical and radiographic criteria of knee OA established by the American College of Rheumatology with a Kellgren and Lawrence score of 2 or greater * Pain score above 3 (range 0-10 on the visual analog scale; higher scores indicate greater pain * Could participate in 4 weeks of treatment and 3 months of follow-up Exclusion Criteria: * Knee OA combined with any infection, inflammation, autoimmune disease, or fracture * History or underlying disease that would affect posture and balance, such as malignancy, dizziness, vertigo, or stroke * Ever underwent any type of knee operation or internal fixation * Pregnant or planning to become pregnant * Receiving other treatment for knee OA in previous 3 months * History of epilepsy, electronic devices implanted in the body * Active infection at the stimulator contact site * Lack of informed consent * Any other reason thought likely to result in inability to complete the trial
Where this trial is running
Taipei, State
- Shin Kong Wu Ho-Su Memorial Hospital — Taipei, State, Taiwan (Recruiting)
Study contacts
- Study coordinator: Yu-Ting Lin, M.D.
- Email: M012225@ms.skh.org.tw
- Phone: +886-28332211
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.