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Clinical Trials/JPRN-UMIN000048119
JPRN-UMIN000048119
Completed
未知

Effects of consumption of the test food on skeletal muscle in healthy Japanese subjects: a randomized, placebo-controlled, double-blind, parallel-group comparison study - Effects of consumption of the test food on skeletal muscle in healthy Japanese subjects

ORTHOMEDICO Inc.0 sites63 target enrollmentJune 22, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Japanese subjects
Sponsor
ORTHOMEDICO Inc.
Enrollment
63
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 22, 2022
End Date
December 26, 2022
Last Updated
last year
Study Type
Interventional
Sex
Male

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 have lactose intolerance 5\. Subjects who use or take "Foods for Specified Health Uses," or "Foods with Functional Claims" in daily 6\. Subjects currently taking medicines (include herbal medicines) and supplements 7\. Subjects who are allergic to medications and/or the test\-food\-related products (particularly milk) 8\. Subjects who are pregnant, breast\-feeding, and planning to become pregnant 9\. Subjects who suffer from COVID\-19 10\. Subjects who cannot perform the specified training 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 the study by the physician

Outcomes

Primary Outcomes

Not specified

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