Study on the arrival of live bifidobacteria in the gastrointestinal tract. -Single group before-after test
- Conditions
- Healthy volunteer
- Registration Number
- JPRN-UMIN000043672
- Lead Sponsor
- KSO Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Not provided
1. Subjects who tend to have loose stools or constipation 2. Subjects who cannot stop the intake of foods containing certain Bifidobacterium from the screening test to the end of the 2-week test. 3. Subjects who are taking drugs that affect digestion and absorption, such as antibiotics 4. Subjects who cannot stop the intake of medicines, quasi-drugs, and health foods that affect the test during the test period. 5. Subjects with food allergies 6. Subjects who consume a large amount of alcohol on a daily basis 7. Subjects who have urgent medical treatment or have serious complications 8. Subjects with digestive disorders or surgical history that affect digestion and absorption and defecation 9. Subjects with a history of irritable bowel syndrome or a current medical history 10. Subjects background Persons who are judged to be inappropriate as subjects based on the answers to the questionnaire 11. Pregnant, willing to become pregnant during the exam, breastfeeding 12. Subjects with a history of drug dependence, alcohol dependence, or current medical history 13. Subjects who have participated in or are willing to participate in tests that take other foods or use drugs, and tests that apply cosmetics and drugs 14. Subjects judged as unsuitable for the study by the investigator for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Detection of certain live Bifidobacterium in feces. Time: Before and after the intervention (0day, 14days)
- Secondary Outcome Measures
Name Time Method Viable cell count of certain Bifidobacterium in feces