ITMCTR2100004644
Recruiting
Phase 1
Clinical observation on the treatment of joint swelling and pain due to the Fengtabuzu syndrome of RA by Dai medicine Longmengshahousan
ConditionsRA
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- RA
- Sponsor
- Yunnan Hospital of Traditional Chinese Medicine
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Meet the 2010 ACR/EULAR DIAGNOSTIC criteria for RA;
- •(2\) It conforms to the diagnostic criteria of Fengtabuzu syndrome;
- •(3\) Between the ages of 18 and 70, regardless of gender;
- •(4\) the hands joint X\-ray stage I and II, joint function class I and II, III;
- •(5\) 2\.6 \< DAS28 \< 5\.1;
- •(6\) Pain or swelling of at least two wrists;
- •(7\) Patients who use hormones, hormone\-suspected substances or biological agents need to stop taking drugs for more than 3 months;
- •(8\) No non\-steroidal anti\-inflammatory drugs or topical analgesics were used at least 1 week before enrollment.
- •(9\) Voluntary subjects signed informed consent.
Exclusion Criteria
- •(1\) Patients with other rheumatic immune diseases, such as systemic lupus erythematosus, Sjogren's syndrome, and severe osteoarthritis;
- •(2\) Complicated with cardiovascular, pulmonary, liver, gastrointestinal, kidney, hematopoietic system or tumor, or complicated with various acute or chronic infections or other infectious diseases (hepatitis, tuberculosis, etc.);
- •(3\) Local skin damage, infection or trauma of the tested joint is not healed;
- •(4\) Those who did not respond to the treatment of methotrexate or leflunomide;
- •(5\) A history of contraindications to experimental drugs (pulmonary interstitial fibrosis, etc.) and allergies;
- •(6\) A history of alcoholism, drug addiction or neuropsychiatric disorders (epilepsy, depression, etc.);
- •(7\) Pregnant or lactating women who have recently had family planning;
- •(8\) Participating in other drug clinical studies.
Outcomes
Primary Outcomes
Not specified
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