None
Conditions
Interventions
Case series:No
Sponsors
Institute of Clinical Pharmacology ,Central South University
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1) Healthy adults; 2) Sign the informed consent.
Exclusion criteria
Exclusion criteria: 1) Age 75 years old; 2) Diagnosed with severe cardiovascular and cerebrovascular diseases, diabetes, chronic kidney disease, malignant tumors and other major diseases; 3) Pregnant women, lactating women, those taking contraceptives; 4) Unwilling to participate in this researcher.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| TMAO; | — |
Secondary
| Measure | Time frame |
|---|---|
| FBG(fasting blood-glucose);SBP;DBP;total cholesterol;triglyceride;high density lipoprotein cholesterol(hdl-c);low density lipoprotein cholesterin;ALT;AST;TBIL;DBIL;UA;SCr;BUN;WBC;Percentage of lymphocytes;Lymphocyte absolute value;Percentage of neutrophils;Neutrophil absolute value;Percentage of monocytes;Monocyte absolute value;Percentage of eosinophils;Eosinophil absolute value;Percentage basophil;Basophil absolute value;RBC;Hb;HCT;MCV;Average hemoglobin content;Average hemoglobin concentration;Erythrocyte volume distribution width - coefficient of variation;Erythrocyte volume distribution width - standard deviation;PLT;Platelet volume;MPV;platelet distribution width; | — |
Countries
China
Contacts
Public ContactDongsheng Ouyang
Institute of Clinical Pharmacology ,Central South University
Outcome results
None listed