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Clinical Trials/JPRN-UMIN000042277
JPRN-UMIN000042277
Completed
未知

Verification of changes in physical condition of citizen runners and blood EPA/AA ratio due to ingestion of gummy candy containing EPA & DHA - Verification of changes in physical condition of citizen runners and blood EPA/AA ratio due to ingestion of gummy candy containing EPA & DHA

Healthcare Systems Co., Ltd.0 sites29 target enrollmentOctober 29, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Healthcare Systems Co., Ltd.
Enrollment
29
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 29, 2020
End Date
February 28, 2021
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\.Persons who are taking drugs such as anticoagulants (e.g., warfarin, edoxaban) during treatment for a specific disease and have decreased hemostatic function 2\.Persons who have been diagnosed with a bleeding disorder and have decreased hemostatic function 3\.Persons who have experienced shock symptoms, allergic symptoms, or anemia when collecting or injecting blood at a medical institution, etc. 4\.Persons who have experienced anemia during normal bleeding 5\.Persons e who usually get red and swollen just by being bitten by a mosquito and do not heal easily 6\.Persons who are currently significantly ill and have weakened immunity 7\.Persons who are allergic to blue fish and gelatin 8\.Persons who regularly use medicines, health foods, and supplements that may affect EPA / AA levels 9\.Persons who participated or planning to participate in other clinical trials / monitor studies (excluding observational studies) within one month before obtaining consent to participate in this study, or after obtaining consent to participate in this study. 10\.Persons who are judged by the principal investigator to be inappropriate for participation in this study

Outcomes

Primary Outcomes

Not specified

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