Postprandial hyperglycemia
Conditions
Interventions
The subjects ingested a single intake of the placebo meal, and injested a single intake of the active meal after 7 days or 14 days.
The subjects ingested a single intake of the active meal, and injest
Sponsors
University of Nagasaki
Nagasaki Prefecture
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Aged more than 20 2) Fasting blood glucose > 82, and < 144 mg/dl 3) Individuals who understand the purpose and contents of the experiment
Exclusion criteria
Exclusion criteria: 1) Individuals taking drugs, supplements and healthy foods which affect the glucose level. 2) Subjects who are contracting kidney and/or liver diseases. 3) Individuals judged to have diabetes mellitus. 4) Individuals with a chronic disease. 5) Person who donated more than 400 ml of blood within 3 months prior to the study. 6) Pregnant women, or women with intending to become pregnant, and lactating women. 7) Individuals participating or intending to participate in a drug administration test. 8) Individuals judged by the doctor to be unsuitable.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postprandial blood glucose (0, 30, 60 and 120 min) | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure, Body weight, BMI | — |
Countries
Japan
Contacts
Public ContactHideki Ito
University of Nagasaki Faculty of Nursing and Nutrition
Outcome results
None listed