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Clinical Trials/JPRN-UMIN000033426
JPRN-UMIN000033426
Completed
未知

Effects of consumption of the test food containing black turmeric (Kaempferia parviflora) extract on fasting blood glucose level, and a verification study for safety evaluation of excessive the test food ingestion in healthy Japanese subjects: a randomized, double-blind, placebo-controlled, parallel-group trial - Effects of consumption of the test food containing black turmeric (Kaempferia parviflora) extract on fasting blood glucose level, and a verification study for safety evaluation of excessive the test food ingestion

ORTHOMEDICO Inc.0 sites30 target enrollmentJuly 18, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy Japanese subjects
Sponsor
ORTHOMEDICO Inc.
Enrollment
30
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 18, 2018
End Date
January 12, 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, myocardial infarction 2\. 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 3\. Subjects who use or take "Foods for Specified Health Uses", "Foods with Functional Claims", or other functional food/beverage in daily \*Particularly taking food/beverage effective in lowering blood sugar in daily 4\. Subjects who are currently taking medications (including herbal medicines) and supplement \*Particularly taking antihypertensive drugs in daily 5\. Subjects who are allergic to medicines and/or the test food related products 6\. Subjects who are pregnant, breast\-feeding, or planning to become pregnant 7\. Subjects who have been enrolled in other clinical trials within the last three months before the agreement to participate in this trial 8\. Subjects who are judged as ineligible to participate in the study by the physician

Outcomes

Primary Outcomes

Not specified

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