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临床试验/JPRN-UMIN000049060
JPRN-UMIN000049060已完成Unknown

A Study of the effects of a test-food on sleep-improving - A Study of the effects of a test-food on sleep-improving

CPCC Company Limited0 个研究点目标入组 40 人开始时间: 2023年9月29日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
40

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- (1) taking in sleep-affecting foods, not less than three times a week (2) who will take medicines which might affect the test (e.g., sleeping pill) during the test period (3) vaccinated within two weeks before this study, or planning to vaccinate during intaking of test-foods (4) with not less than 30.0 kg/m2 of BMI (5) with sleep-apnea syndrome (6) with previous medical history of sleep disorder (7) with a continuous medical treatment for sleep disorder (8) cannot use the sleep-scope during the test period (9) with an alcohol intake at the measurement of brain waves (10) with an overnight trip during the test period (11) with extremely irregular dietary habit/life rhythm (12) with a serious sleep-affecting rhinitis (13) with excessive alcohol intake (14) QIDS-J >=11 (15) with the roomer planning to participate in this study (16) restricting their mealtimes to no more than once a day (not less than once a week), within the last month (17) with medical history of serious diseases (18) with pregnancy, possibly one, or lactating (19) with drug/food allergy (wheat, egg, milk) (20) being fitted with a pacemaker (21) with sensitive skin, irritating by an adhesive tape (22) being under another clinical test (medicine or health food), or participated in that within the last 4 weeks, or will join that after the consent (23) who donated their blood components or blood (0.2 L) within the last month (24) who donated his blood (0.4 L) within the last 3 months (25) who donated her blood (0.4 L) within the last 4 months (26) being collected in total of his blood (1.2 L) within the last 12 months and in this study (27) being collected in total of her blood (0.8 L) within the last 12 months and in this study (28) being determined as ineligible for participation by the principal/sub investigator

研究者

发起方
CPCC Company Limited

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