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Clinical Trials/JPRN-UMIN000041291
JPRN-UMIN000041291
Completed
未知

A verification study for improving cognitive function with the test food in healthy subjects: A randomized double-blind placebo-controlled trial - A verification study for improving cognitive function with the test food in healthy subjects

ORTHOMEDICO Inc.0 sites44 target enrollmentAugust 3, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Japanese subjects
Sponsor
ORTHOMEDICO Inc.
Enrollment
44
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 3, 2020
End Date
July 17, 2021
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. At least one previous medical history of malignant tumor, heart failure or myocardial infarction 2\. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3\. Currently under the treatment for either cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension or other chronic diseases 4\. Subjects who have dementia 5\. Subjects who have mental health issues such as depression disorder, attention deficit/hyperactivity disorder (ADHD), or other issues 6\. Subjects who use or take "Foods for Specified Health Uses", "Foods with Functional Claims", or other functional food/beverage in daily 7\. Subjects who take supplements related to improving cognitive functions, such as docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), ginkgo leaf extract, tocotrienol, astaxanthin, gamma\-aminobutyric acid (GABA), phosphatidylserine, and plasmalogen in daily 8\. Subjects who take blue\-backed fish such as sardines, mackerel, and saury in daily 9\. Subjects who regularly use devices, equipment, and applications that may affect cognitive functions (e.g., brain training puzzles, brain training games) 10\. Currently taking medicines (include herbal medicines) and supplements 11\. Subjects who are allergic to medicines and/or the test food related products 12\. Subjects who are pregnant, breast\-feeding, and planning to become pregnant 13\. Subjects who have been enrolled in other clinical trials within the last three months before the agreement to participate in this trial or plan to enroll in another clinical trial during trial period 14\. Subjects who are judged as ineligible to participate in the study by the physician

Outcomes

Primary Outcomes

Not specified

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