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临床试验/ITMCTR2000004074
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

Xiyuan Hospital, China Academy of Chinese Medical Sciences0 个研究点开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募

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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