ITMCTR2100004992尚未招募1 期
Clinical study on effectiveness and safety of Kunbixiao Decoction optimized by Ersi decoction in the treatment of female rheumatoid arthritis
试验速览
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 18 至 65(—)
- 性别
- Female
入选标准
- •1. Female RA patients who meet the diagnostic criteria of Western medicine and TCM syndrome of ''Toxin Heat Phlegm Stasis Accumulation Syndrome'';
- •2. Aged 18-65 years;
- •3. Disease activity score (DAS28) > 3.2 and <= 5.1;
- •4. Those who did not participate in any drug trials within 4 weeks before enrollment;
- •5. Volunteer subjects and signed informed consent.
排除标准
- •1. Patients who are pregnant, breastfeeding, planning to become pregnant during treatment and/or within 12 weeks after the end of treatment;
- •2. Combined with serious primary diseases such as cardiovascular, liver, kidney and hematopoietic system, mental patients;
- •3. Those who have been diagnosed with other connective tissue diseases such as systemic lupus erythematosus, Sj?gren's syndrome, myositis or dermatomyositis;
- •4. There are pituitary tumors, hyperthyroidism, ovarian cysts and other diseases affecting endocrine, history of uterine or ovarian surgery, or oral contraceptives within the past 4 weeks;
- •5. Those who do not meet the requirements for combined medication;
- •6. Those who are known to be allergic to any traditional Chinese medicine used in this test, or allergic constitution (allergic to two or more drugs, food, and pollen).
- •7. Those with a history of drug, drug or alcohol abuse;
- •8. Other conditions deemed inappropriate by the investigator.
研究者
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