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临床试验/JPRN-UMIN000037893
JPRN-UMIN000037893已完成未知

A confirmation test of the influence for sleep, stress and feeling of fatigue, caused by test food consumption - A confirmation test of the influence for sleep, stress and feeling of fatigue, caused by test food consumption

CPCC Company Limited0 个研究点目标入组 25 人开始时间: 2020年9月4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
25

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 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Subjects who 1.are given continuous treatment by taking medicines. 2.constantly use oral medicines having a possibility of affecting test results. 3.constantly use food having a possibility of affecting test results, such as food for specific health use. 4.have current and/or previous medical history of serious disease. 5.have current and/or previous medical history of sleep disorder. 6.self-aware about their sleep apnea. 7.awake during sleep more than two times a week due to night urination. 8.have allergic rhinitis. 9.use pacemaker. 10.have previous medical history of allergy for medicine and/or food. 11.those BMI are over 30 kg/m2. 12.tend to have skin rash with adhesive tape due to skin hypersensitivity. 13.are pregnant or lactating. 14.have extremely irregular dining and life habits. 15.excessive alcohol intake. 16.are not be able to avoid alcohol intake during test period. 17.are not be able to use electroencephalograph during test period. 18.have plan lodging by travel and/or business trip. 19.are participating the other clinical tests, participated within 4-weeks prior to the current study and/or plan to participate the other clinical tests. 20.donated over 200mL blood and/or blood components within the last one month. And 21.Males who donated over 400mL blood and/or blood components within the last three month. 22.Females who donated over 400mL blood and/or blood components within the last four month. 23.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. 24.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. 25.Others who have been determined ineligible by principal investigator or sub-investigator.

研究者

发起方
CPCC Company Limited

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