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Clinical Trials/JPRN-UMIN000042714
JPRN-UMIN000042714
Completed
未知

Effects of consumption of the test food on maintaining muscular strength in healthy subjects: a randomized, placebo-controlled, double-blind, parallel-group comparison study - Effects of consumption of the test food on maintaining muscular strength in healthy subjects

ORTHOMEDICO Inc.0 sites56 target enrollmentDecember 10, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Japanese subjects
Sponsor
ORTHOMEDICO Inc.
Enrollment
56
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 10, 2020
End Date
September 10, 2021
Last Updated
2 years ago
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 who currently undergoing treatment for any of the following chronic disease: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4\. Subjects who are diagnosed with sarcopenia 5\. Subjects who take ""Foods for Specified Health Uses,"" ""Foods with Functional Claims,"" or other functional food/beverage in daily use 6\. Subjects who currently taking medications (including herbal medicines) and supplements 7\. Subjects who are allergic to medicines and/or the test food related products 8\. Subjects who are pregnant, lactation, or planning to become pregnant 9\. 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 participate another trial during this trial 10\. Subjects who are judged as ineligible to participate in the study by the physician

Outcomes

Primary Outcomes

Not specified

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