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Clinical Trials/JPRN-UMIN000037571
JPRN-UMIN000037571
Completed
未知

A study for evaluating the effect of food containing lactic acid bacteria on relating nasal and ocular symptoms. - A study for evaluating the effect of food containing lactic acid bacteria on relating nasal and ocular symptoms.

TTC Co., Ltd0 sites50 target enrollmentNovember 15, 2020
ConditionsHealthy adult

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy adult
Sponsor
TTC Co., Ltd
Enrollment
50
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 15, 2020
End Date
November 21, 2019
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
TTC Co., Ltd

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\)Subjects who routinely take food or medicine containing lactic acid bacteria or natto bacteria. (2\)Subjects who have severe nasal and eye symptoms affecting judgement of discomfort. (3\)Subjects who routinely take medicines affecting the test result. (4\)Subjects who are under medication (specific desensitization therapy) which may influence the outcome of the study. (5\)Subjects who are engaged in drive a car or operate a hazardous machine. (6\)Subjects judged as unsuitable for the stuzy by the investigator for laboratory evidence or cardiopulmonary function. (7\)Subjects who have a disease requiring regular medication or a history of serious disease for which medication was required. (8\)Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination. (9\)Subjects who are liable to cause an allergy related to the study. (10\)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire. (11\)Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study. (12\)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (13\)Subjects who are judged as unsuitable for the study by the investigator for other reason.

Outcomes

Primary Outcomes

Not specified

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