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Clinical Trials/JPRN-UMIN000024070
JPRN-UMIN000024070
Completed
未知

A study for evaluating the influence on a viability of lactic acid bacteria in intestinal tract due to the difference of form. A randomized, single-blind trial. - A study for evaluating the influence on a viability of lactic acid bacteria in intestinal tract due to the difference of form.

KSO Corporation0 sites16 target enrollmentSeptember 16, 2016

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy volunteers
Sponsor
KSO Corporation
Enrollment
16
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 16, 2016
End Date
October 16, 2016
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Individuals with a loose stool and/or a tendency for constipation Individuals taking in common use (2\) Individuals taking antiflatulents and/or laxatives (including purgative drug) and/or health foods in common use, including food for specified health use (3\) Individuals taking antibiotics and/or drugs which influence laxatives(including purgative drugs) in common use (4\) Individuals who are not able to stop consumption of foods containing lactic acid bacteria, bifidobacteria, natto bacteria, oligosaccharides, dietary fibers, high amount of sugar alcohol and/or other health foods including food for specified health use, which influence intestinal regulation during the study period (5\) Individuals presenting known food allergy (6\) Individuals taking large amounts of alcohol on a daily basis (7\) Individuals who are suffered from a disease which needs treatment urgently or individuals with severe complications (8\) Individuals with a digestive organ disease or surgical history who has an influence on digestive absorption and defecation (9\) Individuals who are under treatment or have a history of irritable bowel syndrome (10\) Individuals who are judged to be unsuitable as a subject from an answer of a subjective background questionnaire (11\) Individuals who are pregnant or breast\-feeding, or have the will of pregnancy during the study period (12\) Individuals who are under treatment or have a history of drug/alcohol dependence (13\) Individuals who participate in other clinical studies or who are in willing to participate to these studies using foods, drugs and/or cosmetics (14\) Individuals who are judged as unsuitable for the study by the investigator for the other reasons

Outcomes

Primary Outcomes

Not specified

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