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临床试验/JPRN-UMIN000053958
JPRN-UMIN000053958已完成Unknown

A verification study of elevation of postprandial blood glucose level: an open-label study - A verification study of elevation of postprandial blood glucose level

ORTHOMEDICO Inc.0 个研究点目标入组 22 人开始时间: 2024年3月25日最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
22

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 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

研究者

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