Pain Relief Effect of Low-intensity Continuous Ultrasound Stimulator for Knee Arthritis
Osteoarthritis, Knee
About this trial
This is an interventional treatment trial for Osteoarthritis, Knee
Eligibility Criteria
Inclusion Criteria: Patients aged 40 to 60 years with pain due to OA of the knee and able to walk voluntarily Those who have more than one osteophyte in the tibiofemoral joint on radiographic findings (Kellgren-Lawrence gradesⅡ,Ⅲ) At visit 1 (screening) and visit 2, the pain status during knee OA activity was 100 mm pain VAS, as a result, those who are over 40mm If the Kellgren & Lawrence Grades are the same, target the one with the higher 100mm pain VAS Patients who are willing or able to follow the doctor's instructions, including joint movements Persons who can comply with concomitantly permitted drugs, prohibited drugs, and relief drugs Persons who can maintain the same exercise and activity during the clinical trial period Fully understand the purpose and procedure of this clinical trial Exclusion Criteria: Those who have a history of rheumatoid arthritis or gouty arthritis or who have peripheral pain other than the knee joint patient. Those with fractures or dislocations on simple radiological examination. Those who are identified, or those with a similar risk of neuromuscular disease Those who have participated in other clinical trials within 6 months of participating in clinical trials. Patients with severe pain in the knee joint other than angular deformity, instability, and index knee in the knee joint Patients with other tumors other than degenerative knee arthrosis Persons with systemic symptoms that may affect knee pain Pregnant and lactating women
Sites / Locations
- Wonju College of Medicine
Arms of the Study
Arm 1
Other
Treatment group
Single treatment group for evaluation pain relief before and after LICUS treatment