None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) men and women over the age of 50 2) A person who falls under the ACR criteria 'clinical and radiological findings (II)', has pain in the knee joint, and is accompanied by crude stiffness and creptus + osteophytes that last less than 30 minutes 3) Knee osteoarthritis of Grade 2 or higher according to the Kellgren-Lawrence grading scale (K-L grade) according to x-ray examination 4) Of the bilateral knee joints, A person who has pain in the knee joint at least one joint 5) A person whose pain scale (VAS) of 40 mm or more has lasted for more than 6 months during activity and rest 6) A person who voluntarily submitted a written consent form and signed the consent form for participation in clinical trials without any problems in reading and writing Korean 7) A person with a prevalence period of degenerative knee osteoarthritis for more than 3 months
Exclusion criteria
Exclusion criteria: 1) a person unable to walk due to knee pain 2) In the case of knee surgery accompanied by loss of connective tissue around the knee 3) Patients with rheumatoid arthritis or other metabolic arthritis 4) A person who has received injections such as steroids or prologue therapy around the joint cavity or knee within 3 months of screening, or who is taking drugs for the purpose of treating osteoarthritis 5) Those who need attention to invasive laser needle procedures or sedimentation stimulation (those with hemicoagulant disorders, severe skin diseases at the treatment site, those with a metallic device in the knee area, and those with implantable devices such as a pacemaker) 6) Subjects who are vulnerable by definition by the clinical trial review committee of the medical institution where the clinical trial is conducted 7)You're pregnant, or you're pregnant The one who prepares 8) A person who determines that the tester is unfit to participate in clinical trials due to other reasons 9) who are participating in another clinical trials 10) A person who receives medical treatment as part of social insurance, compensation and compensation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Variation of 100mm pain scale (VAS) at 5 weeks compared to Baseline;Adverse event;Skin condition and vital signs;Blood test | — |
Secondary
| Measure | Time frame |
|---|---|
| Variation of 100mm pain scale (VAS) at 1-5 weeks relative to Baseline;Changes in the knee knee osteoarthritis symptom assessment (KOOS) score at 1-5 weeks compared to Baseline;Change in Quality of Life Assessment (EQ-5D-5L) score at 1-5 weeks compared to Baseline;Changes in general health (PGA) scores from 1 to 5 weeks compared to Baseline | — |
Countries
Korea, Republic of
Contacts
Dongshin University Mokpo Oriental Hospital