None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Voluntarily agree to participate and signed in informed consent form 2) Adults aged over 20 years 3) Plasma total cholesterol levels = 200mg/dl and < 250mgl/dl
Exclusion criteria
Exclusion criteria: 1) Continuous consumption of drug or dietary supplement that affect lipid metabolism within 4 weeks before the first visit (statin, fibrate, beta-blocker, etc) 2) Following diseases: ? Myocardial infarction, stroke, uncontrolled hypertension (= 140/90mmHg) ? Diabetes (fasting plasma glucose = 126mg/dl) ? Liver failure(AST, ALT rose more than 2.5 times the upper limit of normal) ? Renal impairment (Creatinine = 1.4mg/dl) ? Hyperthyroidism and hypothyroidism ? Malignant tumors 3) Familial hypercholesterolemia 4) Participation in another clinical trial within 4 weeks of first visit 5) Alcoholic 6) Pregnant or lactating women 7) Hypersensitivity to chlorella 8) Any condition that the principal investigator belives may put the subjects at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma total cholesterol levels | — |
Secondary
| Measure | Time frame |
|---|---|
| Triglycerides,LDL-cholesterol,HDL-cholesterol,VLDL-cholesterol,Total cholesterol/HDL-cholesterol, HDL-cholesterol/LDL-cholesterol,ApoA1,ApoB,ApoE,LCAT,CETP,carotenoids,fastingbloodglucose, etc | — |
Countries
Korea, Republic of
Contacts
Ewha Womans University