Effects of consumption of the test food on cognitive function of healthy Japanese subjects: A randomized double-blind placebo-controlled trial - Effects of consumption of the test food on cognitive function of healthy Japanese subjects

ORTHOMEDICO Inc.0 sites66 target enrollmentJune 30, 2020

Overview

Phase: 未知
Intervention: Not specified
Conditions: Not specified
Sponsor: ORTHOMEDICO Inc.
Enrollment: 66
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

June 30, 2020

End Date

December 12, 2020

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

ORTHOMEDICO Inc.

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\. Currently taking medicines (include herbal medicines) and supplements 10\. Subjects who are allergic to medicines and/or the test food related products 11\. Subjects who are pregnant, breast\-feeding, and plan to become a pregnant during the study period or in the future, or wish for their own child 12\. 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 anther clinical trial during trial period 13\. Subjects who are judged as ineligible to participate in the study by the physician