JPRN-UMIN000042014已完成未知
Verification of the effects of test food on vascular endothelium functionality and gut environment - Verification of the effects of test food on vascular endothelium functionality and gut environment
CPCC Company Limited0 个研究点目标入组 36 人开始时间: 2021年10月23日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 36
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 are currently receiving medication. (2) Subjects who have a plan or who have taken medication which would affects the trial result (drug for intestinal disorder, antihypertensive, laxative or antibiotics) within a month before the trial start. (3) Subjects who are regularly consuming food for specified health uses (FOSHU), food with function claims, supplement and/or health foods which would affects the trial results for more the 3 times per week. (4) Subjects who are breast-feeding, pregnant, and are planning pregnancy. (5) Subjects who have current medical history/anamnesis of severe cardiac, hepatic, renal or digestive diseases. (6) Subjects who are heavy use of alcohol. (7) Subjects who have history of smoking. If subject have quit smoking for more than a month prior to trial, the subject could be included. (8) Subjects with irregular life style and diet. (9) Subjects who have allergies to food or medication. (10) Subjects who are currently participating, or who have been participated to other study for medicine or food within the last 4 weeks of the trial, or who possibly participate to other clinical trial after agreement of this study. (11) Subjects who donated over 200mL blood and/or blood components within a month to the current study. (12) Males who donated over 400mL blood and/or blood components within the last 3 months to the current study. (13) Females who donated over 400mL blood and/or blood components within the last 4 months to the current study. (14) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last 12 months are adding to the planned sampling amounts of this study. (15) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last 12 months are adding to the planned sampling amounts of this study. (16) Others who have been determined ineligible by principal investigator or sub-investigator.
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