Exploratory study on changes in the intestinal environment during synbiotics intake.
- Conditions
- one
- Registration Number
- JPRN-UMIN000054030
- Lead Sponsor
- Morinaga Milk Industry Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 100
Not provided
1. Subjects who regularly use medicine that affect the gut microbiota, such as intestinal regulators, laxatives, etc 2. Subjects who unable to stop ingestion of foods and supplements containing bifidobacteria, oligosaccharide, etc. 3. Subjects with serious disorders on hepatic, kidney, cardiac, lung, digestive organs, blood, endocrine system, mental and metabolic system, or related severe past medical histories 4. Subjects with medication allergy, food allergy, or serious history of these 5. Subjects who have milk allergy or lactose intolerance 6. Subjects who are pregnant, under lactation or expecting to be pregnant during this study 7. Subjects who participated in other study within 1 month prior to obtaining informed consent 8. Any candidates considered to be inappropriate for this study by the principal investigator based on their background etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method