ITMCTR2000004074尚未招募未知
Study on dose-effect relationship and safety of Modified Huangqi Chifeng Decoction with different doses of Astragalus in the treatment of IgA nephroproteinuria
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
- 性别
- All
入选标准
- •1. The diagnosis was IgA nephropathy, and the pathologic reports of renal perforation were reported in all cases;
- •2. No gender limitation, aged 18-70 years;
- •3. Moderate proteinuria(24-hour urinary protein quantity is between 1.0-2.5g)accompanied or not accompanied by microscopic hematuria;
- •4. CKD1-2 (GFR>=60ml/min/1.73m2);
- •5. TCM syndrome differentiation accords with qi deficiency and blood stasis syndrome as well as wind pathogen and heat toxicity;
- •6. Non-dialysis patients with infection, acidosis, electrolyte disturbance, hypertension and other aggravating factors are effectively controlled and the condition is stable. The BP is between 130-90/80-60mmHg. Potassium is in the normal range;
- •7. Voluntarily accept this study and sign the informed consent form.
排除标准
- •1. Secondary factors leading to proteinuria, such as purpura nephritis, lupus nephritis;
- •2. Patients who have been treated by glucocorticoid, immunosuppressant, tripterygium wilfordii preparation in three months are not included;
- •3. Having mental illness, infectious disease or lactation, pregnancy or planned pregnancy during the study period;
- •4. Patients complicated with serious diseases of the heart, brain, liver and hematopoietic system, or other serious diseases affecting their survival;
- •5. Patients with unilateral or bilateral renal artery stenosis;
- •6. Participants who are participating in other interventional clinical trials.
研究者
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