A randomized controlled study of floating needle in the treatment of knee osteoarthritis
- Conditions
- Knee osteoarthritis
- Registration Number
- ITMCTR2200006055
- Lead Sponsor
- The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
(1) Those who meet the diagnostic criteria of the American rheumatic Society for knee arthritis and are confirmed by X-ray films;
(2) Grade I, II and III patients meeting the radiological diagnostic criteria of Kellgren lawrecne;
(3) Between 40-80 years old, regardless of gender;
(4) Those who have not taken other relevant drugs or adopted relevant treatment methods within 1 week (those who have taken drugs for a long time need to stop taking drugs for 1 week before they can be included in the observation);
(5) Volunteer to participate, sign the informed consent form, and be willing to accept the test.
(1) Pregnant women or persons suffering from major diseases or infectious diseases;
(2) Patients with a history of fracture, dislocation, tuberculosis, tumor, infection, etc. in the knee joint (the condition of such patients may affect the observed treatment results);
(3) Those who are allergic to the medical devices (such as floating needles) involved in this test;
(4) Mental illness, lack of self-control, unable to express accurately;
(5) Those who participated in other clinical trials 3 months before the trial;
(6) The educational level is too low to understand the contents of the test or scale.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method WOMAC Osteoarthritis Index;
- Secondary Outcome Measures
Name Time Method Three dimensional gait;X-ray;Musculoskeletal ultrasound;VAS score;