None listed
Conditions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subject who voluntarily agrees to participate and sign in informed consent form 2) Man and women (20 years = Age < 65 years) 3) Fasting blood sugar level <126 mg/dL
Exclusion criteria
Exclusion criteria: 1) Volunteer who has taken medicine, herbal medicine or dietary supplement to affect glucose metabolism within 1 months 2) BMI < 18.5kg/m2 or = 30 kg/m2 3) Volunteer who treatment for following disease: diabetes mellitus, liver complaint, renal disease, thyroid gland disease, cardiovascular disease, hypertension 4) Volunteer who have a good quality of diet 5) high-intensity exercise regularly 6) Volunteer who had a weight change of more than 4 kg within 4 weeks or is on weight control therapy 7) Volunteer who drink continuously 8) Excessive smokers 9) Volunteer who has been in clinical demonstration within 1 month 10) Pregnant woman, lactating women or planning to pregnant 11) Volunteer who are hypersensitivity or allergy to dietary supplement or ingredients contained in the supplement. 12) Volunteer who judged incongruent by tester through clinical examination center
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postprandial blood glucose levels and related biomarkers | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse reaction, vital signs | — |
Countries
Korea, Republic of
Contacts
Seoul National University of Science and Technology