JPRN-UMIN000046745已完成未知
An exploratory study on the effect of continuous intake of test food on vascular functions. -a single-arm, open-label trial- - An exploratory study on the effect of continuous intake of test food on vascular functions
IMEQRD Co., Ltd.0 个研究点目标入组 10 人开始时间: 2022年2月8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
- 10
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 59years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Those who are currently undergoing treatment for any disease, or who receive medical treatment such as medical drugs or traditional Chinese medicines. However, medications used as needed will be allowed to join the trial. 2.Those who have been receiving nutritional and exercise therapy under medical doctors. 3.Those who have severe diseases or a history of severe diseases. 4.Those who have severe anemia. 5.Those who have currently been taking commercially available drugs, quasi-drug products, foods, or supplements with any functional claims. However, Those who can discontinue taking these drugs/foods during the trial period will be allowed to join the trial. 6.Those who have currently been utilizing any medical machines, such as warmth medical treatment, to improve fatigue, mental/physical stress, coldness, blood flow, blood pressure. However, Those who can discontinue using these machines during the trial period will be allowed to join the trial. 7.Those who have a cold allergy, a drug allergy, or a food allergy. 8.Those who smoke within one year before the trial. 9.Those who drink more than 60 g alcohol/day. 10.Women who have abnormal menstrual periods, or during menstruation on the day of visit. 11.Those who donated blood more than 400 mL (men) or 200 mL (women) within three months before the trial. 12.Those who are planning extremely change their lifestyle (such as diet, sleep, or exercise) during the study period. 13.Those who work in shift and night shift. 14.Those who are planning travel to foreign countries during the study period. 15.Those who are currently pregnant or breastfeeding, or planning to pregnant during the study period. 16.Those who joined other clinical trials from one month before the trial, or Those who have currently been joined other clinical trials. Also, Those who are planning to join other clinical trials during the trial. 17.Those who are unsuitable for this study, that judged by the principal investigator.
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