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Clinical Trials/JPRN-UMIN000031366
JPRN-UMIN000031366
Completed
N/A

Effect on cognitive function. - Effect on cognitive function.

CPCC Company Limited0 sites14 target enrollmentFebruary 19, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Healthy subjects
Sponsor
CPCC Company Limited
Enrollment
14
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 19, 2018
End Date
October 30, 2018
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
CPCC Company Limited

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Subjects who constantly use medicines, supplements having a possibility of affecting test results. 2\) Subjects who have previous and/or current medical history of serious disease such as cerebral infarction, cerebrovascular disease, psychosis, dementia and so on. 3\) Subjects who excessive alcohol intake and excess smoker. 4\) Subjects who have extremely irregular dining habits, and subjects who have midnight work or irregular shift work. 5\) Subjects who have previous medical history of drug and/or food (especially gelatin) allergy. 6\) Subjects who are participating the other clinical tests. Subjects who participated within 4\-weeks prior to the current study and/or who plan to participate the other clinical tests. 7\) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. 8\) Males who donated over 400mL blood and/or blood components within the last three month to the current study. 9\) Females who donated over 400mL blood and/or blood components within the last four month to the current study. 10\) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. 11\) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. 12\) Subjects who are positive for infectious. 13\) Others who have been determined ineligible by principal investigator or sub\-investigator.

Outcomes

Primary Outcomes

Not specified

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