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Clinical Trials/JPRN-UMIN000031101
JPRN-UMIN000031101
Completed
未知

A confirmation study for improving effects of probiotics and synbiotics on intestinal environment in healthy adults. - A confirmation study for improving effects of probiotics and synbiotics on intestinal environment.

KSO Co., Ltd0 sites60 target enrollmentJune 30, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Subjects with a tendency for constipation
Sponsor
KSO Co., Ltd
Enrollment
60
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 30, 2019
End Date
May 7, 2018
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Subjects who regularly use intestinal drugs and laxatives (including strong laxatives). 2\. Subjects who regularly intake healthy food to relieve constipation. 3\. Subjects who use medicine such as antibiotics that affect digestion and absorption. 4\. Subjects who can't stop intake food containing viable bacteria such as Lactic acid bacteria, Bifidobacteria, Natto bacteria and/or enhanced with oligosaccharide, dietary fiber and/or the health food to relieve constipation (including Food for Specified Health Uses (FOSHU)) and/or containing a large amount of sugar alcohol during this study. 5\. Subjects who have allergic to food. 6\. Subjects who have serious diseases requiring an urgent treatment, or who accept severe complication. 7\. Subjects who has a medical history of diseases or surgeries affecting digestion, absorption and bowel movement. 8\. Subjects are judged unsuitable for this study based on subject questionnaire. 9\. Subjects who is pregnant or willing to be pregnant or breast\-feeding during this study 10\. Subjects who has a current or history of drug dependence and/or alcoholism. 11\. Subjects who are participated in other clinical trials that intake/apply any of food, drug, and cosmetics, or willing to be that 12\. Subjects who are judged unsuitable for this study by principal investigator

Outcomes

Primary Outcomes

Not specified

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