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Clinical Trials/JPRN-UMIN000051045
JPRN-UMIN000051045
Completed
未知

A verification study of the improving effects of the test food consumption on cognitive function: a randomized, placebo-controlled, double-blind, parallel-group comparison study - A verification study of the improving effects of the test food consumption on cognitive function

ORTHOMEDICO Inc.0 sites56 target enrollmentMay 12, 2023
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ConditionsHealthy Japanese subjects

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Japanese subjects
Sponsor
ORTHOMEDICO Inc.
Enrollment
56
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 12, 2023
End Date
December 23, 2023
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • •1\. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2\. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3\. Subjects currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any 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," or "Foods with Functional Claims" in daily 7\. Subjects who are currently taking medications (including herbal medicines) and supplements 8\. Subjects who usually use devices, equipment, and applications that may affect cognitive functions (e.g., brain training puzzles, brain training games) 9\. Subjects who are allergic to medicines and/or the test food related products 10\. Subjects who are pregnant, lactating, or planning to become pregnant during this trial 11\. Subjects who have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 12\. Subjects who are judged as ineligible to participate in this study by the physician

Outcomes

Primary Outcomes

Not specified

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