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临床试验/ITMCTR2200006490
ITMCTR2200006490尚未招募1 期

Evaluation of clinical effect of compound Shelong Capsule on urinary protein in membranous nephropathy

Shanxi Hospital of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方

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

年龄范围
16 至 65(—)
性别
All

入选标准

  • (1) Consistent with the clinical diagnosis of chronic nephritis and stage I-II pathological diagnosis of membranous nephropathy;
  • (2) TCM syndrome differentiation belongs to the syndrome of mutual obstruction of dampness and stasis;
  • (3)0.3g/24h= 24h urinary protein quantification <3.5g/24h;
  • (4) Serum creatinine =176µmol/L, or glomerular filtration rate (GFR)= 60mL /(min·1.73m2);
  • (5) Aged between 16 and 65, regardless of gender;
  • (6) Acute aggravating factors such as infection, electrolyte disturbance, severe hypertension, hyperlipemia and hyperglycemia can be effectively controlled;
  • (7) Those who voluntarily participate in the experiment and sign the informed consent.

排除标准

  • (1) Patients with serious primary diseases of the heart, brain, liver and hematopoietic system, type 1 diabetes, or other serious diseases affecting their survival;
  • (2) 24-hour urine protein quantification =3.5g/24h or < 0.4g/24h;
  • (3) serum creatinine =177µmol/L, or serum creatinine clearance (GFR)<60ml/(min·1.73m2);
  • (4) pregnant or lactating women;
  • (5) Persons with allergic constitution who have a history of drug allergy or are known to be allergic to the drug components in the test;
  • (6) Those who are taking similar study drugs or antihypertensive drugs with protein-lowering effect or are currently taking hormone or immunosuppressive therapy;
  • (7) mentally ill or legally disabled persons;
  • (8) Those who have no fixed place to work and are easy to fall off;
  • (9) Participants in another clinical drug trial.

研究者

发起方
Shanxi Hospital of Traditional Chinese Medicine

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