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A verification study of elevation of postprandial blood glucose level

Not Applicable
Conditions
Healthy Japanese
Registration Number
JPRN-UMIN000053958
Lead Sponsor
ORTHOMEDICO Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
22
Inclusion Criteria

Not provided

Exclusion Criteria

1. Individuals who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. Individuals who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. Individuals who are currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, chronic kidney disease, cerebrovascular disorder, rheumatic disease, diabetes mellitus, dyslipidemia, hypertension, gastrointestinal disorder, or any other chronic diseases 4. Individuals who usually drink to excess (average of more than about 20 g/day as absolute alcohol intake) {500 mL: a medium bottle of beer or about 1.5 cans of canned chu-hi, 180 mL: 1 go of sake or about 1.5 glasses of wine, 90 mL: half-go with shochu, 60 mL: a glass of whiskey brandy (double)} 5. Individuals who are a smoker 6. Individuals who have irregular sleeping time or habit due to work such as a late-night shift 7. Individuals who have irregular lifestyles 8. Individuals who are taking "Foods for Specified Health Uses" or "Foods with Functional Claims" 9. Individuals who are taking or using medications (including herbal medicines) and supplements 10. Individuals who are allergic to medicines and/or the test product related products (particularly, eggs, wheat, buckwheat, milk ingredients, pork, chicken, beef, peanuts, soybeans, squid, shrimp, mackerel, salmon, sesame, apple, peach, and gelatin) 11. Individuals who are pregnant, lactating, or planning to become pregnant during this study 12. Individuals who have been enrolled in other clinical studies within the last 28 days before the agreement to participate in this study or plan to participate another study during this study 13. Individuals who are judged as ineligible to participate in this study by the physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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