Effects of grain constituent on postprandial hyperglycemia : placebo-controlled double blind cross-over trial
Not Applicable
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000017447
- Lead Sponsor
- QOL RD Co.,Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 23
Inclusion Criteria
Not provided
Exclusion Criteria
1) Subjects who take continuous medical treatment. 2) Subjects who are contracting heart disease, liver disease, kidney disease, digestive disease and allergy disease. 3) Subjects with serious infection 4) Subjects with smoking habit 5) Those whose amount of drinking on the 1st is more than 500 ml in beer conversion. 6) Subjects who are doing carbohydrates restricted diet now. 7) Subjects who participate in other clinical trials. 8) Subjects who are not eligible due to physician's judgment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood samples were collected before ingestion and 0.5,1,2,3,4 and 5 hours after ingestion.Urine samples were collected before ingestion and accumulation urine samples were pooled during the postprandial reriods for 5 hrs. Primary outcome is postprandial blood glucose
- Secondary Outcome Measures
Name Time Method Key secondary outcomes are insulin, triglyceride and glucose-dependent insulinotropic polypeptide.