None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subject who voluntarily agrees to participate and signs in informed consent form 2) Age: = 30 years 3) BMI: = 23kg/m2 and < 30kg/m2 4) Plasma LDL cholesterol levels = 130mg/dl
Exclusion criteria
Exclusion criteria: 1) Continuous consumption of dietary supplements or medicine which can affect antioxidative capacity within 4 weeks before the first visit 2) Continuous consumption of Lycium barbarum within 4 weeks before the first visit 3) Continuous administration of drugs which can affect antioxidative capacity within 4 weeks before the first visit (hypolipidemic, antiinflammatory drug, hypotensive, antibiotics, aspirin, hypoglycemic, anticoagulant) 4) Subject with following diseases and past medical history within 2 years before the first visit (Hypertension, diabetes, atherosclerosis, chronic inflammatory disease, CVD, renal disease, liver disease, thyroid disease, malignant tumor, mental illness) 5) Subject who loses weight over 4kg within 30 day before the first visit 6) Consumption of alcohol (= 140g/week) 7) Smoker (= 10 cigarettes/day) 8) Excessive exercise (= 7 hours/week) 9) Pregnant women, lactating women, or menopausal women with hormone therapy 10) Participation in other human study within 4 weeks before the first visit 11) Subjects with hypersensitivity to test materials 12) Any condition that the principal investigator believes may put the subjects at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Antioxidative markers | — |
Secondary
| Measure | Time frame |
|---|---|
| Lipid profiles, etc. | — |
Countries
Korea, Republic of
Contacts
Ewha Womans University