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临床试验/JPRN-UMIN000044060
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Confirmation research on sleep improvement by ingestion of a black tea ingredient-containing tablet - Confirmation research on sleep improvement by ingestion of a black tea ingredient-containing tablet

CPCC Company Limited0 个研究点目标入组 44 人开始时间: 2022年4月29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
44

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 46years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) Subjects who do not care for a black tea very much. (2) Subjects with smoking habit. (3) Subjects being over-sensitiveness to cold, even during the summer season. (4) Subjects with nasal congestion during this trial. (5) At present, subjects with continuous medical treatment. (6) Subjects having present/previous medical history of serious diseases in liver, kidney, heart, lung, and/or blood. (7) Subjects with a remedy for their sleep disorder. (8) Subjects with high blood pressure--max of above 160 mmHg, min of above 100 mmHg--. (9) Subjects who have any difficulty in refraining from taking steadily in the health-specific/functional/health foods, which might affect their sleep during this trial. (10) Subjects who realized that the subjects themselves must be in a state of menopausal disorder. (11) Subjects planning to go on a trip, or to stay in places except homes. (12) Subjects with any difficulty in refraining from using a smartphone/cellphone/personal computer, an hour before going to bed. (13) Subjects who have any difficulty in refraining from alcohol and/or caffein, after 17 o'clock during this trial. (14) Subjects sleeping together with their family (especially in pre-school children) in a bed time. (15) Pregnant, possibly pregnant, or lactating women. (16) Subjects donated their blood components and/or whole blood (200 mL) within a month to this trial. (17) Males donated their whole blood (400 mL) within the last three months to this trial. (18) Females donated their whole blood (400 mL) within the last four months to this trial. (19) Males being collected in total of their blood (1200 mL) for the last twelve months plus in this trial. (20) Females being collected in total of their blood (800 mL) for the last twelve months plus in this trial. (21) Subjects being under the other clinical tests, or took part in those within a month before this trial. (22) Others as ineligible for participation, determined by the principal investigator's opinions.

研究者

发起方
CPCC Company Limited

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