None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Those who agreed to participate in this study and signed a written consent form 2) Adult men and women over the age of 20 3) Those whose blood triglyceride level is less than 200 mg/dL
Exclusion criteria
Exclusion criteria: 1) Those who have the following diseases or have a history - Hyperlipidemia, uncontrolled diabetes/hypertension, liver disease, kidney disease, intestinal disease (including inflammatory bowel disease and lactose intolerance), cardiovascular/cerebrovascular disease, malignant tumor, gastrointestinal disease requiring treatment, thyroid disease, pancreatitis, multiple Multiple sclerosis, anemia, dementia, depression, anorexia, bulimia, asthma, other allergic diseases, etc. 2) If you have taken the following medications within 3 months of your first visit or are expected to take them during the study period - Drugs that affect fat absorption or lipid metabolism (lipid-lowering drugs, etc.), hypoglycemic agents, drugs that affect insulin secretion/activity, hormones, anticoagulants, etc. 3) If you are on hormone replacement therapy 4) If you have continuously taken herbal medicines within 2 months of your first visit 5) Those who donated blood within 3 weeks of their first visit 6) Those who have continuously consumed health functional foods (plant sterols, omega-3 fatty acids, psyllium husk, aloe, etc.) that can affect blood sugar, lipid, and body fat metabolism within 1 month of the first visit 7) Those with good meal quality (Recommended Food Score > 36) 8) Vegetarian 9) Alcoholics or those who usually consume more than 420 g/week of alcohol (about 7 bottles/week of soju) 10) Those with a body mass index (BMI) of 23 kg/m2 or less or 35 kg/m2 or more 11) Those who are losing weight or who have had a weight change of 10% or more within 3 months of their first visit 12) Those who regularly engage in high-intensity exercise (=10 hours/week) 13) Excessive smokers (=20 cigarettes/day) 14) Those who participated in another clinical study within 1 month of the first visit 15) Pregnant or lactating women, those who plan to become pregnant 16) Those who have hypersensitivity to the ingredients contained in the test/control food or who have experienced a severe food allergy reaction 17) Those who are judged inappropriate by the researcher to participate in this research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Triglycerides | — |
Secondary
| Measure | Time frame |
|---|---|
| APO-B 100 | — |
Countries
Korea, Republic of
Contacts
Seoul National University of Science and Technology