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 ? 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) BMI: <18kg/m2 and = 30kg/m2 5) Participation in another clinical trial within 4 weeks of first visit 6) Alcoholic 7) Any condition that the principal investigator belives may put the subjects at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood lipid profile (total cholesterol, LDL-cholesterol, HDL-cholesterol, VLDL-cholesterol) | — |
Secondary
| Measure | Time frame |
|---|---|
| Inflammatory biomarker (CRP, TNF-a) | — |
Countries
Korea, Republic of
Contacts
The Catholic University of Korea Catholic Medical Center