None listed
Conditions
Sponsors
Meiji Co., Ltd
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Healthy adults range in age from 20 to 40 at the time of informed consent. 2. Subjects whose defecation frequency are more than 3 times a week 3. Subjects with a BMI of 18.5 or more and less than 25. 4. Subjects who agree to participate in this study with a written informed consent after receiving sufficient explanation relating to this study.
Exclusion criteria
Exclusion criteria: 1. Subjects with food allergies 2. Subjects who suffer from serious disorders of liver, kidney, heart, lung, digestive organs (including gastric resection), diabetes, rheumatoid arthritis, neurological/mental diseases, endocrine diseases, or other serious and/or progressive diseases. 3. Heavy drinkers (weekly average of 30 g / day or more of pure alcohol) 4. Smoker 5. Subjects who regularly take supplements and health foods for intestinal function or containing prebiotics (e.g. Oligosaccharide, dietary fiber) 6. Subjects who are currently pregnant or breastfeeding, or who wish to become pregnant during the test period. 7. Subjects who donated more than 200ml blood within the past 1 month 8. Subjects who participate in other clinical trials within the past 3 months or have plans to participate in other clinical trials during this study period 9. Subjects who determine ineligible by the principal investigator or the co-investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Breath hydrogen concentrations | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood glucose level, Gastrointestinal hormone(PYY), VAS (Hunger, Fullness, Desire-to-eat, Prospective Food Consumption, Thirst, Comfort) | — |
Countries
Japan
Contacts
Public ContactYoshitaka Kawai
Meiji Co., Ltd. R&D Division
Outcome results
None listed