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临床试验/ITMCTR2000003313
ITMCTR2000003313招募中1 期

Randomized double-blind parallel controlled clinical trail of Chenpi enzyme in the treatment of hyperlipidemia

Guangdong Province Traditional Chinese Medical Hospital0 个研究点开始时间: 待定最近更新:
适应症

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. Patients aged 18-75 years;
  • 2. Patients with dyslipidemia;
  • 3. The cardiovascular risk was assessed as low risk patients;
  • 4. Those who voluntarily participate in the research and sign the informed consent.

排除标准

  • 1. Patients who were taking antilipidemic drugs within 3 months before inclusion;
  • 2. Patients with nephrotic syndrome, hypothyroidism, renal failure, liver disease and systemic lupus erythematosus;
  • 3. Patients with myeloma, glycogen accumulation, fatty atrophy, acute porphyria and polycystic ovary syndrome;
  • 4. Patients taking drugs related to lipid metabolism, such as diuretics, beta blockers, glucocorticoids, metformin, insulin and contraceptives;
  • 5. Patients whose systolic blood pressure is still >= 180mmhg or diastolic blood pressure is still >= 110mhg after treatment;
  • 6. After oral drug treatment, the blood glucose is still >= 11.1mmol/L Of patients;
  • 7. TG >= 5.65mmol/L Those who;
  • 8. Patients with heart, liver, kidney, hematopoietic system, immune system and other systemic serious diseases;
  • 9. Pregnant or lactating women or those who plan to be pregnant during the trial period or their spouses plan to be pregnant;
  • 10. Patients with allergic constitution, possible allergy to the drug or psychosis;
  • 11. Other patients who cannot cooperate for a long time.

研究者

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