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临床试验/JPRN-UMIN000051176
JPRN-UMIN000051176已完成Unknown

Preliminary evaluation of the efficacy of plant-derived component on vascular endothelial function - The effect plant-derived component on vascular endothelial function

KAGOME CO., LTD.0 个研究点目标入组 75 人开始时间: 2023年5月26日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
75

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
40years-old 至 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Subjects who have a chronic disease and are undergoing treatment 2) Subjects with a history or current medical history of serious liver disease, kidney disease, gastrointestinal disease, heart disease, respiratory disease, endocrine disease, thyroid disease, adrenal disease, or other metabolic disease 3) Subjects diagnosed with arrhythmia at the screening test 4) Subjects who are judged unsuitable for this study based on the screening test 5) Subjects who have a history of gastrointestinal disease or gastrointestinal surgery that affects digestion and absorption 6) Subjects who have allergies to drugs or foods (especially test foods) 7) Subjects who cannot stop taking a supplement or a supplement/healthy food that may affect vascular endothelial function or blood pressure during the study period 8) Subjects who consume foods containing a large amount of the plant-derived component 3 times a week or more 9) Subjects who was collected more than 200 mL of blood within 1 month or 400 mL of blood within 3 months prior to the date of informed consent 10) Subjects who have a history of drug dependence or alcohol dependence 11) Subjects who drink 20 g or more of pure alcohol per day for 3 days or more a week 12) Subjects who smoke 21 or more cigarettes per day on average (including e-cigarettes) 13) Shift worker or late night worker 14) Subjects who are pregnant or who intend to become pregnant during the study period or who are breastfeeding 15) Subjects who are participating in research that takes other foods or medicines, applies cosmetics or medicines or who have participated in other research within one month prior to the date of informed consent or who are willing to participate in other research 16) Subjects who are judged unsuitable for this study by the investigator, principal researcher or researchers

研究者

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