Pilot study on pharmacokinetics of tea ingredients
- Conditions
- healthy adults
- Registration Number
- JPRN-UMIN000051709
- Lead Sponsor
- kyoto prefectural university of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 10
Not provided
1.Subjects with serious liver disorder, cardiovascular disorder, respiratory disorder, endocrine disorder, metabolic disorder 2.Subjects who may have an allergic reaction to tea or test food 3.Subjects who are pregnant, breastfeeding, or intend to become pregnant during the study period 4.Irregular menstrual cycle 5. Persons with extremely irregular eating habits, shift workers, late-night workers 6.Subjects who have collected more than 200 mL of blood within 1 month or more than 400 mL within 3 months before the start of this study (blood donation, etc.) 7.Subjects who regularly use pharmaceuticals (including herbal medicines) and supplements 8.Those who cannot agree with the purpose of the explanation of the test conducted in advance. 9.In addition, those who are judged to be inappropriate for this study by the study supervisor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood concentration and saliva concentration of tea polyphenols
- Secondary Outcome Measures
Name Time Method