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临床试验/ITMCTR2200006576
ITMCTR2200006576尚未招募1 期

Study on The Intervention Effect on Patients with Dyslipidemia of Dampness Syndrome

Guangdong Provincial Hospital of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

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
18 至 70(—)
性别
All

入选标准

  • 1.18-70 years old.
  • 2.Those who meet the typical diagnosis of dampness syndrome in the Diagnostic Standard of Dampness Syndrome of Traditional Chinese Medicine V2.0.
  • 3.Those who meet the diagnosis of dyslipidemia in the guidelines for Prevention and Treatment of Dyslipidemia in Chinese Adults (2016 revised Edition).
  • 4.Patients whose cardiovascular risk assessment is medium risk and low risk.
  • 5.Those who volunteer to participate in the study of this subject and sign informed consent forms.

排除标准

  • 1. Patients with nephrotic syndrome, hypothyroidism, renal failure, liver disease, systemic lupus erythematosus, myeloma, glycogen accumulation, lipoatrophy, acute porphyria and polycystic ovary syndrome.
  • 2. Patients who are using drugs related to blood lipid metabolism, such as diuretics, beta blockers, glucocorticoids, metformin, insulin, contraceptive.
  • 3. Patients with systolic blood pressure = 180mmHg or diastolic blood pressure = 110mHg after treatment.
  • 4. Patients whose fasting blood glucose was still = 11.1mmol/L after oral drug treatment.
  • 5. Patients whose TG = 5.65mmol/L.
  • 6. Patients with systemic severe diseases such as heart, liver, kidney, hematopoietic system, immune system, etc.
  • 7. Pregnant or lactating women or people who plan to become pregnant during the trial or whose spouse plans to become pregnant.
  • 8. Patients with allergic constitution, who may be allergic to this drug or who are mentally ill.
  • 9. Other patients who can't cooperate for a long time.

研究者

发起方
Guangdong Provincial Hospital of Chinese Medicine

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