JPRN-UMIN000037706已完成未知
A confirmation test of effects for improvement of blood flow and cold sensitivity by test food consumption - A confirmation test of effects for improvement of blood flow and cold sensitivity by test food consumption
CPCC Company Limited0 个研究点目标入组 60 人开始时间: 2020年4月1日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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
- 30years-old 至 64years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Subjects who are diagnosed as cold sensitivity by medical doctor (2) Smokers except who have quitted smoke more than twelve months before the day of consent. (3) Subjects who regularly use blood pressure, blood flow, fatigue and/or cold sensitivity improving medicines, healthy foods (foods for specified health use, functional indication foods) and /or supplements. (4) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period. (5) Subjects who have previous and/or current medical history of serious disease (e.g., heart, liver, kidney, digestive organ). (6) Subjects who excessive alcohol intake. (7) Subjects who have extremely irregular dining habits, and subjects who have midnight work or irregular shift work. (8) Subjects who have previous medical history of drug and/or food allergy. (9) Subjects who have cold allergy. (10) Subjects who prone to diarrhea include who are diagnosed lactose intolerance (11) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. (12) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. (13) Males who donated over 400mL blood and/or blood components within the last three month to the current study. (14) Females who donated over 400mL blood and/or blood components within the last four month to the current study. (15) Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (16) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (17) Others who have been determined ineligible by principal investigator or sub-investigator.
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