Investigation on change with time of blood polyphenol concentration after its oral administratio
Not Applicable
- Conditions
- ormal healthy subjects
- Registration Number
- JPRN-UMIN000030619
- Lead Sponsor
- SAPPORO HOLDINGS Ltd. Frontier Laboratory for Value Creation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 8
Inclusion Criteria
Not provided
Exclusion Criteria
1.Persons receiving medications such as uric acid levels, hypertension, diabetes, etc. 2.Persons who are allergic to the test food 3.Pregnancy, breast-feeding, or pregnancy planning person 4.Those who are scheduled to undergo surgery / hospitalization, etc. for two months before and after the examination period (November 2017 to February 2018) 5.Persons who are judged unsuitable for participating in this trial by the principal investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method