Knee cartilage injury
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults over the age of 18 and under the age of 60, regardless of gender. 2. Symptoms, signs and imaging changes are in line with localized ? degree cartilage defect of knee joint or chondromalacia patella, patellofemoral joint cartilage injury, mild to moderate knee osteoarthritis. 3. Other treatment methods are ineffective. 4. No other knee cartilage defect treatments will be performed during the trial period. 5. Subjects must be able to communicate well with investigators and comply with the requirements of the research, and must give written, signed and dated informed consent before any research-related activities. All relevant legal representatives will also sign written research consents in accordance with local laws and regulations.
Exclusion criteria
Exclusion criteria: 1. Subjects with cartilage defect diameter = 160mmHg and/or diastolic blood pressure >= 95mmHg), congestive heart failure (New York Heart Association status class III or IV). 12. Subjects with serum creatinine levels exceeding 2.0 mg/dl (176.8 µmol/L). 13. Total white blood cell (WBC) count at screening <2500/µL, or platelets <100000/µL or neutrophils <1500/µL or hemoglobin <8.5 g/dL. 14. Pregnant or lactating women, pregnancy is defined as the state of a woman after conception until termination of pregnancy, confirmed by a positive hCG laboratory test result. 15. Females of childbearing potential, defined as all females who are biologically capable of becoming pregnant unless they use an effective method of contraception throughout the duration of study treatment administration. 16. History of alcohol or drug abuse or evidence of ongoing abuse within six months prior to baseline.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MOCART score; | — |
Secondary
| Measure | Time frame |
|---|---|
| WOMAC score;VAS score;IKDC score; | — |
Countries
China