Unique ID issued by UMIN | UMIN000053204 |
---|---|
Receipt number | R000060721 |
Scientific Title | Evaluation of the effect of test food intake on the gut environment due to the gut environment type |
Date of disclosure of the study information | 2023/12/22 |
Last modified on | 2024/07/29 19:40:57 |
Evaluation of the effect of test food intake on the gut environment due to the gut environment type
Evaluation of the effect of test food intake on the gut environment due to the gut environment type
Evaluation of the effect of test food intake on the gut environment due to the gut environment type
Evaluation of the effect of test food intake on the gut environment due to the gut environment type
Japan |
Healthy male/female adults
Not applicable | Adult |
Others
NO
To evaluation of the effect of test food intake on the gut environment due to the gut environment type
Safety,Efficacy
Gut metabolites
Gut microbiota
Defecation status
POMS2
Athens Insomnia Scale
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Prevention
Food |
Consumption of any of test food No. 1 to 5 with milk for 8 weeks
20 | years-old | <= |
65 | years-old | > |
Male and Female
(1) At informed consent, male/female subjects aged more than or equal to 20, and less than 65 years old.
(2) Subjects who are members of Calomama app.
(3) Subjects who get into a habit of having breakfast, and will be able to replace their breakfast by the test food.
(4) Subjects who can collect and send fecal samples to the analysis agency.
(5) Subjects who can show their understanding of the study procedure and agreement with participating in the study by written informed consent prior to the study.
(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.
100
1st name | Shinnosuke |
Middle name | |
Last name | Murakami |
Metagen, Inc.
Headquarters
997-0052
246-2 Mizukami, Kakuganji, Tsuruoka, Yamagata, Japan
+81-235-64-0330
research@metagen.co.jp
1st name | Makoto |
Middle name | |
Last name | Ichinohe |
CPCC Company Limited
Clinical Planning Department
103-0021
4F Daiwa Building, 3-3-10 Nihonbashi-Hongokucho, Chuo-ku, Tokyo, Japan
+81-3-6225-9001
cpcc-contact@cpcc.co.jp
Metagen, Inc.
Calbee, Inc.
Profit organization
Institutional Review Board of Chiyoda Paramedical Care Clinic
2F Daiwa Building, 3-3-10 Nihonbashi-Hongokucho, Chuo-ku, Tokyo 103-0021, Japan
+81-3-6225-9005
IRB@cpcc.co.jp
NO
2023 | Year | 12 | Month | 22 | Day |
Unpublished
Completed
2023 | Year | 12 | Month | 18 | Day |
2023 | Year | 12 | Month | 15 | Day |
2023 | Year | 12 | Month | 25 | Day |
2024 | Year | 06 | Month | 17 | Day |
2023 | Year | 12 | Month | 22 | Day |
2024 | Year | 07 | Month | 29 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000060721