研究疾病:
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糖尿病肾病微量白蛋白尿期
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研究疾病代码:
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Target disease:
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Microalbuminuria of Diabetic Nephropathy in Patients with Type 2 Diabetes.
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Target disease code:
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研究类型:
Study type:
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干预性研究
Interventional study
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研究设计:
Study design:
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随机平行对照
randomized controlled trial(parallel group design)
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研究所处阶段:
Study phase:
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上市后药物
Post-marketing clinical trial
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研究目的:
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评价芪蛭降糖胶囊对2型糖尿病肾病微量白蛋白尿期气阴两虚兼瘀证患者的尿微量白蛋白/肌酐比、肾小球滤过率(eGFR)、肌酐、尿素氮(BUN)、血糖、血脂四项、血压、中医证候及症状积分的疗效,同时评价药物的安全性(血、尿、便常规、肝功能、心电图、不良事件),为DKD的中医治疗提供临床证据。
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Objectives of Study:
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To evaluate the urinary microalbumin/creatinine ratio, glomerular filtration rate (eGFR), creatinine, and urea nitrogen (BUN) ,the efficacy of blood glucose, blood lipids, blood pressure, TCM syndromes and symptom scores in patients with type 2 diabetic nephropathy, microalbuminuria, qi and yin deficiency syndrome , as well as the safety of drugs (blood, urine, stool routine, liver function, electrocardiogram, adverse events), provide clinical evidence for the treatment of DKD.
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药物成份或治疗方案详述:
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本实验研究纳入患者200例,随机分为4组,每组50例患者,具体给药方案如下:
A组:芪蛭降糖胶囊,5粒/次,3次/日,口服,温开水送服
B组:芪蛭降糖胶囊安慰剂,5粒/次,3次/日,口服,温开水送服
C组:西医对症治疗(建议ACEI或ARB类药物)的基础上,加用芪蛭降糖胶囊,5粒/次,3次/日,口服,温开水送服。
D组:西医对症治疗(建议ACEI或ARB类药物)的基础上,加用芪蛭降糖胶囊安慰剂,5粒/次,3次/日,口服,温开水送服。
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Description for medicine or protocol of treatment in detail:
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Group A: QiZhiJiangTang capsules, 5 capsules pertime, tid, po, warm water delivery service;
Group B: QiZhiJiangTang capsules placebo, 5 capsules pertime, tid, po, warm water delivery service;
Group C: Western medicine symptomatic treatment (recommended ACEI or ARB drugs)+ QiZhiJiangTang capsules, 5 capsules pertime, tid, po, warm water delivery service;
Group D: Western medicine symptomatic treatment (recommended ACEI or ARB drugs) + QiZhiJiangTang capsules placebo, 5 capsules pertime, tid, po, warm water delivery service.
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纳入标准:
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(1)符合糖尿病肾脏疾病微量白蛋白尿期的诊断标准;
(2)年龄30~70岁;
(3)中医辨证为气阴两虚兼瘀证;
(4)签署患者知情同意书。
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Inclusion criteria
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(1) Diagnostic criteria for microalbuminuria in diabetic kidney disease;
(2) Aged 30 to 70 years;
(3) TCM syndrome differentiation is the combination of Qi and Yin;
(4) Sign the patient's informed consent form.
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排除标准:
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(1)合并有心血管、肝、肾和造血系统等严重原发性疾病,血清转氨酶大于正常值的2倍,血清肌酐大于正常值上限,精神病患者。
(2)妊娠、准备妊娠或哺乳期妇女,或有药物过敏史者。
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Exclusion criteria:
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(1) Combined with serious primary diseases such as cardiovascular, liver, kidney and hematopoietic system, serum transaminase is more than twice the normal value, serum creatinine is greater than the upper limit of normal, and patients with mental illness.
(2) Pregnancy, preparation for pregnancy or lactation, or history of drug allergy.
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研究实施时间:
Study execute time:
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从From
2019-01-01
至To
2021-12-31
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征募观察对象时间:
Recruiting time:
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从From
2019-06-01
至To
2019-12-01
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