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临床试验/JPRN-UMIN000048921
JPRN-UMIN000048921已完成Unknown

A study for evaluating effects of a single intake of the test beverage on EEG and autonomic nervous system. - A study for evaluating effects of a single intake of the test beverage on EEG and autonomic nervous system.

HUMA R&D CORP0 个研究点目标入组 24 人开始时间: 2023年9月12日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
24

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
20years-old 至 35years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Subject who is taking medication or under medical treatment due to illness. 2.Subject who is taking foods for specified health use, foods with functional claims, health foods (including supplements) that affect the autonomic nervous system, metabolism, and sleep, and cannot stop taking them during the test period. 3.Subject who is out of the hospital due to mental disorders (depression, etc.) or sleep disorders, or who has a history of mental illness in the past. 4.Subject with a history of serious diseases such as heart, liver, kidneys, digestive organs, brain, malignant tumors, immune diseases, diabetes, etc. 5.Subject with defects in EEG and heart rate measurements (abundance chest hair, use of a pacemaker, skin rash, etc.) 6.Heavy drinker. 7.Subject who has difficulty quitting drinking from the day before the test date. 8.Subject who has extremely irregular eating habits, those who work shifts, those who work late at night, etc. 9.Subject who is participating in other clinical trials at the time of obtaining consent, and who plans to participate in other clinical trials within 4 weeks from the end of the study to the start of the main study of the study, or after consenting to participate in the study. 10.Subject who is likely to be under great stress due to moving, changing jobs, separation from close relatives, etc. within the last 3 months. 11.Subject who exercises violently on a daily basis. 12.Subject with severe PMS (premenstrual syndrome) symptoms. 13.Subject who is planning to get pregnant during the test period after the day of informed consent or is currently pregnant and lactating. 14.Subject with hay fever or allergic rhinitis (seasonal or perennial) 15.Subject who is allergic to medicines and food. 16.Subject who has or had a history of either medicine or alcohol. 17.Subject who can't keep the daily records. 18.Subject who the investigator has determined that participation in this study is inappropriate.

研究者

发起方
HUMA R&D CORP

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