Evaluation of the effect of test food intake on the gut environment due to the gut environment type
- Conditions
- Healthy male/female adults
- Registration Number
- JPRN-UMIN000053204
- Lead Sponsor
- Metagen, Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 100
Not provided
(1) Subjects who have a plan or who have taken medication within a month before the pre-test start, which would affect the intestinal environment. (2) Subjects who had undergone appendectomy. (3) Subjects who have received the surgery which would affect the trial result within half a year before obtaining a consent. (4) 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. (5) Subjects having an irregular meal rhythm. (6) Subjects who take excessive alcohol. (7)Subjects whose roomer is planning to join this trial. (8) Subjects who are planning to change their life style considerably during this trial. (9) Subjects who cannot drink milk. (10) Subjects who have previous/current medical history of severe cardiac, hepatic, renal or digestive diseases. (11) Pregnant, possibly pregnant, or lactating women. (12) Subjects with lactose intolerance. (13) Subjects who have food allergies. (14) Others who have been determined ineligible by principal/sub investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method