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
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