JPRN-UMIN000045573已完成Unknown
Study on sleep-improving effects by test-food intakes - Study on sleep-improving effects by test-food intakes
CPCC Company Limited0 个研究点目标入组 16 人开始时间: 2022年10月1日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 16
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) with the roomer planning to participate in this study, (15) restricting their mealtimes to no more than once a day (not less than once a week), within the last month, (16) with medical history of serious diseases, (17) with pregnancy, possibly one, or lactating, (18) with drug/food allergy (wheat, egg, milk), (19) being fitted with a pacemaker, (20) with sensitive skin, irritating by an adhesive tape, (21) 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, (22) who donated their blood components or blood (0.2 L) within the last month, (23) who donated his blood (0.4 L) within the last 3 months, (24) who donated her blood (0.4 L) within the last 4 months, (25) being collected in total of his blood (1.2 L) within the last 12 months and in this study, (26) being collected in total of her blood (0.8 L) within the last 12 months and in this study, (27) being determined as ineligible for participation by the principal/sub investigator - - .
研究者
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