Gastrointestinal Microbiome Clinical Trial
— Vigiis101Official title:
Effects of Vigiis 101-LAB on Gut Health
Verified date | August 2019 |
Source | SunWay Biotech Co., LTD. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Vigiis 101-LAB capsules I and II are produced from the fermentation of Lactobacillus paracasei subsp. paracasei NTU 101. Investigators have examined the effects of the Vigiis 101-LAB capsules I or II (5 or 10 billion CFU/day, respectively) on gut microflora in clinical trial 1, and on peristalsis, related immunity, and anti-oxidative capacity in clinical trial 2, during a 4-week randomized, double-blind, placebo-controlled, adaptive-design study.
Status | Completed |
Enrollment | 54 |
Est. completion date | March 20, 2018 |
Est. primary completion date | December 22, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Healthy adults aged ? 20 years and ? 65 years. - Subjects with normal weight (body mass index: 18.5-24). - Subjects with no gastrointestinal diseases or on medication. Exclusion Criteria: - Pregnant or lactating women. - Subjects who are allergic to Lactobacillus. - Subjects with chronic gastrointestinal diseases. - Subjects who previously underwent gastrectomy or gastric bypass. - Subjects with liver, kidney, or heart disease, alcoholism, or uncontrolled diabetes. - Subjects who developed stroke, psychiatric diseases, or depression within the last 1 year. - Subjects being administered drugs that can regulate gastrointestinal function, functional foods, bacteriostatic drugs or supplements, antibiotics, antioxidants, or other unknown drugs within the last 2 weeks. - Patients who did not fulfill the inclusion criteria, did not administer the test product according to regulations, whose efficacy could not be determined, or who had incomplete data that affect efficacy or safety assessment. |
Country | Name | City | State |
---|---|---|---|
Taiwan | Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine | Taipei |
Lead Sponsor | Collaborator |
---|---|
SunWay Biotech Co., LTD. | Chung Shan Medical University, National Taiwan University Hospital |
Taiwan,
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* Note: There are 49 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Gut Microflora | Outcome measurements: Analysis of correlation between stool frequency and gut microbiota change of the gut microbiome will be calculated at 4 week in comparison with admission. |
4 week | |
Primary | Peristalsis intestine | Analysis of correlation between chyme passage time through the gut at 4 and 6 week in comparison with admission. | 6 week |
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