A study to investigate the effects of a 4-week intake of the test food on the intestinal environment and the disposition of the test food after a single intake of the test food.
- Conditions
- Healthy male adults
- Registration Number
- JPRN-UMIN000051814
- Lead Sponsor
- Metagen, Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Male
- Target Recruitment
- 16
Not provided
(1)Subjects who have a plan or who have taken the food containing quercetin within a month before the trial start or during the trial. (2)Subjects who have a plan or who have taken medication within a month before the pre-test start or during the trial, which would affect the trial result. (3)Subjects who had undergone appendectomy. (4)Subjects who have received the surgery which would affect the trial result within half a year before obtaining a consent. (5)Subjects who are expected to undergo major changes in their living environment such as home and work during this trial. (6)Subjects with irregular dietary habits. (7)Subjects who take excessive alcohol. (8)Subjects whose roomer is planning to join this trial. (9)Subjects who are now under other clinical tests with some kind of medicine/food, or participated in those within 4 weeks before this trial, or will join those after giving informed consent to participate in this trial. (10)Subjects who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (11)Subjects who are allergic to medicines and test foods (related to lactic acid bacteria). (12)Subjects who donated their blood components, and/or whole blood 200 mL within a month before the trial start. (13)Subjects who donated their blood components, and/or whole blood 400 mL within 3 months before the trial start. (14)Subjects whose collected blood volume within the last 12 months before the trial start would reach to 1,200 mL after adding the blood collection in this study. (15) Others who have been determined ineligible by the principal/sub investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method