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Clinical Trials/JPRN-UMIN000036551
JPRN-UMIN000036551
Completed
未知

A verification study of anti-obesity effects of the test food: an open-label trial - A verification study of anti-obesity effects of the test food

ORTHOMEDICO Inc.0 sites0 target enrollmentApril 20, 2019

Overview

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

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 20, 2019
End Date
August 10, 2019
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\. Currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disease, kidney disease, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4\. Subjects who receive hormonal therapy 5\. Subjects who are planning to undergo a surgical operation within two weeks from the date of finish of the intervention period 6\. Subjects who use or take "Foods for Specified Health Uses", "Foods with Function Claims", or other functional food/beverage in daily 7\. Subjects who have habits of excessive exercise 8\. Subjects who are currently taking medications (including herbal medicines) and supplements. Particularly taking an antidiabetic drug in daily. 9\. Subjects who are allergic to medicines and/or the test food related products 10\. Subjects who are pregnant, lactation, or planning to become pregnant 11\. 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 12\. Subjects who are ineligibility to participate in the study based on the evaluation of the principal physician

Outcomes

Primary Outcomes

Not specified

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