osteoarthritis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) The subjects voluntarily agree to participate in the study and sign a written informed consent; (2) Age 18-75 years old, male or female; (3) According to clinical diagnosis, the patient has been diagnosed with unilateral osteoarthritis. According to the Kellgren Lawrence imaging grading, grades 0 to I belong to the early stage; Grade II-III belongs to the mid-term stage; Grade IV belongs to the late stage, and this study selected grades II-III with VAS>40mm; (4) No previous bleeding, asthma, severe cardiac, liver and renal insufficiency, non-steroidal drug allergy history;
Exclusion criteria
Exclusion criteria: (1) previous treatment that may affect the efficacy; (2) Patients with open wounds, scars or ulcers in the gel paste application area; (3) There are fractures, dislocations, etc. present; Accompanied by serious primary diseases such as tumors, cardiovascular and cerebrovascular diseases, hematological disorders, or accompanied by mental illness and communication disorders, the efficacy cannot be determined. Radiation pain or activity disorders caused by other diseases (visceral organ lesions, cardiovascular and cerebrovascular diseases); (4) Pregnant and lactating women or women of childbearing age who are trying to conceive; (5) Other situations in which the researcher considers it inappropriate to participate in this experiment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effective rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS score;WOMAC score;Knee Lysholm score;Adverse reaction observation; | — |
Countries
China
Contacts
Zhejiang Hospital of Traditional Chinese Medicine