|
研究疾病:
|
类风湿关节炎
|
研究疾病代码:
|
|
|
Target disease:
|
rheumatoid arthritis
|
Target disease code:
|
|
研究类型:
Study type:
|
干预性研究
Interventional study
|
研究设计:
Study design:
|
随机平行对照
randomized controlled trial(parallel group design)
|
|
研究所处阶段:
Study phase:
|
探索性研究/预试验
Pilot clinical trial
|
|
研究目的:
|
运用多组学技术筛选类风湿关节炎的生物学特征,证实清热解毒祛湿通络法治疗类风湿关节炎(湿热毒蕴证)的有效性和安全性。
|
|
Objectives of Study:
|
Using multi omics techniques to screen the biological characteristics of rheumatoid arthritis, the effectiveness and safety of the method of clearing heat, detoxifying, dispelling dampness, and promoting collaterals in treating rheumatoid arthritis (damp heat toxin accumulation syndrome) were confirmed.
|
|
药物成份或治疗方案详述:
|
1.用法用量:
试验组:清热解毒祛湿通络法方剂,水煎服,一日一剂,2次/日;联合甲氨蝶呤12.5~15 mg,每周1次;
对照组:甲氨蝶呤12.5~15 mg,每周1次;
2.疗程:12周。
|
|
Description for medicine or protocol of treatment in detail:
|
1. Usage and dosage:
Experimental group: Formula for clearing heat, detoxifying, dispelling dampness, and promoting collaterals, decocted in water and taken orally, one dose per day, twice a day; Combined methotrexate 12.5-15 mg, once a week;
Control group: Methotrexate 12.5-15 mg, once a week;
2. Course of treatment: 12 weeks.
|
|
纳入标准:
|
(1)符合类风湿关节炎西医诊断标准;
(2)符合中医类风湿关节炎湿热毒蕴证的诊断标准;
(3)符合类风湿关节炎活动期判断标准,即DAS28>3.2(其中C反应蛋白(CRP)和血沉(ESR)可任选其中一个指标进行计算,本研究选用ESR指标);
(4)18岁≤年龄≤80岁;
(5)受试者同意加入本次研究,并签署知情同意书;
|
|
Inclusion criteria
|
(1) Meets the Western diagnostic criteria for rheumatoid arthritis;
(2) Meets the diagnostic criteria for rheumatoid arthritis with dampness heat toxin syndrome in traditional Chinese medicine;
(3) Meets the criteria for determining the active phase of rheumatoid arthritis which is DAS28>3.2 (where C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) can be selected as one of the indicators for calculation and ESR was used in this study);
(4) 18 years old ≤ 80 years old;
(5) The subjects agree to join this study and sign an informed consent form;
|
|
排除标准:
|
(1)入组前1个月内使用治疗 RA 相关的免疫抑制类、激素类药物的患者;
(2)合并银屑病关节炎、强直性脊柱炎、痛风等炎性关节炎疾病者;
(3)合并严重的心脑血管、肺、肾、内分泌和造血系统等原发性疾病者;
(4)有乙型肝炎、丙型肝炎、结核病、艾滋病病史或获得性免疫缺陷综合症(AIDS)病史、恶性肿瘤病史者;
(5)肝肾功能严重异常者;
(6)对试验药物成分过敏者;
(7)妊娠、准备妊娠或哺乳期妇女;
(8)近1月内参加过或正在参加其他临床试验者;
(9)精神性疾病,无自知力,无法确切表达或不能按时服药,不能配合完成试验者。
|
|
Exclusion criteria:
|
(1) Patients who have used immunosuppressive and steroid drugs related to RA treatment within one month prior to enrollment;
(2) Patients with combined inflammatory joint diseases such as psoriatic arthritis, ankylosing spondylitis, gout, etc;
(3) Individuals with severe primary diseases of cardiovascular, pulmonary, renal, endocrine, and hematopoietic systems;
(4) Have a history of hepatitis B, hepatitis C, tuberculosis, AIDS, acquired immunodeficiency syndrome (AIDS), or malignant tumor;
(5) Individuals with severe abnormalities in liver and kidney function;
(6) Individuals who are allergic to the components of the experimental drug;
(7) Pregnant, preparing for pregnancy or breastfeeding women;
(8) Individuals who have participated or are currently participating in other clinical trials within the past month;
(9) Mental illness, lack of self-awareness, inability to express accurately or take medication on time, and inability to cooperate in completing the trial.
|
|
研究实施时间:
Study execute time:
|
从From
2024-07-29
至To
2025-07-29
|
征募观察对象时间:
Recruiting time:
|
从From
2024-07-29
至To
2025-07-29
|