Chinese Medicine Prevention and Treatment Program for Pre-clinical Rheumatoid Arthritis: An Evidence-based Evaluation Study
- Conditions
- Rheumatoid Arthritis
- Registration Number
- ITMCTR1900002430
- Lead Sponsor
- Zhejiang Chinese Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
1) Patients should suffer from >=1 arthritis (joint pain with swelling) and ACPA-positive, but do not meet the classification criteria of 1987 ACR RA classification criteria nor the 2010 ACR/EULAR RA classification criteria or other RA classification criteria;
2) The duration of diseases should last 6 weeks to 6 months;
3) Patients should meet the criteria of the patent of spleen deficiency and blockage of wind and damp;
4) Patients aged 18 to 65 years;
5) Patients will be well informed and agree to participate in this study.
1) Patients were treated with DMARDs or hydroxychloroquine within 2 months when agreeing to participate in this study;
2) Patients were treated with glucocorticoids;
3) Patients who suffer from severe organ disease or mental illness;
4) Patients who are allergic or have contraindications to the drugs involved in the study.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method RA transition rate;
- Secondary Outcome Measures
Name Time Method Patent scores;Simplified disease activity index, SDAI;patient's global assessment ofdisease activity, PGA;Clinical disease activity index, CDAI;physician's global assessment of disease activity, MDGA;Visual Analogue Scale/Score, VAS;