ITMCTR2200006576
Not yet recruiting
Phase 1
Study on The Intervention Effect on Patients with Dyslipidemia of Dampness Syndrome
Guangdong Provincial Hospital of Chinese Medicine0 sitesTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Guangdong Provincial Hospital of Chinese Medicine
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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