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Clinical Trials/JPRN-UMIN000043543
JPRN-UMIN000043543
Completed
未知

Human intervention trial on the effect of long-term ingestion of dry powdered ecklonia stolonifera from Nishinoshima-chou on the reduction of nasal and eye discomfort - Human intervention trial on the effect of long-term ingestion of dry powdered ecklonia stolonifera from Nishinoshima-chou on the reduction of nasal and eye discomfort

Healthcare Systems Co., Ltd0 sites60 target enrollmentMarch 8, 2021
ConditionsHealthy Adults

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Adults
Sponsor
Healthcare Systems Co., Ltd
Enrollment
60
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 8, 2021
End Date
July 31, 2021
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\.Persons who have chronic illness, receiving medication, have a serious disease history (diabetes, liver disease, kidney disease, heart disease, respiratory disease, endocrine disease, etc.) 2\.Persons who have allergy to the test food (ecklonia stolonifera), shrimp and crab. 3\.Persons who regularly take test food (ecklonia stolonifera). 4\.Persons who regularly take seaweed, foods containing seaweed or supplements. 5\.Persons who are seeing or planning to see an otorhinolaryngologist. 6\.Persons who have been diagnosed with acute rhinitis, sinusitis, or hypertrophic rhinitis. 7\.Persons who have been diagnosed with bronchial asthma. 8\.Persons who have severe anemia, alcoholism, or other mental disorders. 9\.Persons who have a smoking habit. 10\.Persons who regularly use medicines, specified health foods, or health foods that may affect nasal or eye discomfort. 11\.Persons who may change their lifestyle during the study period (e.g., working at night, traveling for long periods of time). 12\.Persons who plan to take new health foods or supplements during the study period. 13\.Persons who have participated in other studies during the month prior to the start of the study, or persons who plan to participate in other studies after consenting to this study. 14\.Persons who have been judged ineligible by the study supervising physician or principal investigator. 15\.Persons who are breast\-feeding, pregnant, or who plan or wish to become pregnant during the study period.

Outcomes

Primary Outcomes

Not specified

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