研究疾病:
|
难治性痛风
|
研究疾病代码:
|
|
Target disease:
|
Refractory gout
|
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:
|
从代谢组学角度,检测难治性痛风组(反复急性发作且西药难以控制)与健康组血清及粪便代谢标记物变化差别,结合证候研究,分析上述检测结果的与“阴火”内在联系,为证候研究提供实质实验基础。同时经中药治疗后,再次评估患者中医证候积分、症状积分分级量化指标、炎症因子(血沉、CRP、TNF-α、IL-6),寻找中医治疗的可能机制或作用靶点。
|
Objectives of Study:
|
From the perspective of metabonomics, the changes of serum and fecal metabolic markers in refractory gout group (repeated acute attacks and difficult to control by Western Medicine) and healthy group were detected. Combined with syndrome research, the internal relationship between the above detection results and "Yin Fire" was analyzed to provide substantial experimental basis for syndrome research. At the same time, after TCM treatment, TCM syndrome score, symptom score grading quantitative index, inflammatory factors (ESR, CRP, TNF - α, IL-6) were evaluated again to find the possible mechanism or target of TCM treatment.
|
药物成份或治疗方案详述:
|
1)中药治疗组:原来西药治疗方案+中药汤剂;
中药汤剂药物组成:黄芪 20 克、当归 10 克、防风 10 克、地骨皮 20 克、知母 10 克、桂枝 15 克、赤芍 20 克 黑顺片(熟附子)10 克 炙甘草 10 克 、广升麻 15 克、白术20 克、乌梅 20 克、细辛 5 克、燀桃仁 10 克等。药物来源:东莞市中医院。
用法:日 1 剂,水煎至 400ml,分早晚两次温服,治疗共 10 天
2)非中药治疗组:原来西药治疗方案+小剂量泼尼松(10-15mg qd)。
|
Description for medicine or protocol of treatment in detail:
|
1) Traditional Chinese medicine treatment group: the original western medicine treatment scheme + traditional Chinese medicine decoction;
Composition of traditional Chinese medicine decoction: Huangqi 20g, Danggui 10g, Fangfeng 10g, Digupi 20g, Zhimu 10g
Guizhi 15g, Chishao 20g, heishun tablets (ripe aconite) 10g, Zhigancao 10g, guangshengma 15g, Baizhu 15g
20 g, 20 g black plum, 5 g asarum, 10 g peach kernel, etc. Drug source: Dongguan Hospital of traditional Chinese medicine.
Usage: 1 dose per day, decoct to 400ml, take warm twice in the morning and evening for 10 days
2) Non traditional Chinese medicine treatment group: the original western medicine treatment scheme + small dose prednisone (10-15mg QD).
|
纳入标准:
|
(1)符合上述中西医诊断标准。
(2)年龄 18-70 岁。
(3)急性期予常规西药非甾体消炎止痛药和治疗 5 天仍未缓解。
(4)依从性好,能按规范接受治疗及各项检测。
|
Inclusion criteria
|
(1) The above diagnostic criteria were met.
(2) They were 18-70 years old.
(3) In the acute stage, the patients were treated with conventional western medicine, non steroidal anti-inflammatory analgesics and 5 days of treatment.
(4) Good compliance, can receive treatment and testing according to the standard.
|
排除标准:
|
妊娠或哺乳期妇女及精神病患者;内分泌疾病患者;合并重度营养不良,或伴有心、脑、肾、造血系统严重损害者;合并其他风湿病的患者。不能配合研究流程患者。
|
Exclusion criteria:
|
Pregnant or lactating women and psychiatric patients; patients with endocrine diseases; patients with severe malnutrition or severe damage to heart, brain, kidney and hematopoietic system; patients with other rheumatic diseases. Can not cooperate with the research process.
|
研究实施时间:
Study execute time:
|
从From
2021-01-01
至To
2023-12-31
|
征募观察对象时间:
Recruiting time:
|
从From
2021-03-01
至To
2023-02-28
|