JPRN-UMIN000048293已完成未知
Effect of Daily Ingestion of Test Food on Improving Sleep Quality: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study - Effect of Daily Ingestion of Test Food on Improving Sleep Quality
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 90
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
- •1.Subjects who are under physician's advice, treatment, and/or medication for insomnia, depression, Parkinson's disease, mood disorder, sleep apnea syndrome, nocturnal polyuria, prostatic hypertrophy, overactive bladder, hypertension, dyslipidemia and/or diabetes, etc. 2.Subjects who frequently go to the toilet at night. 3.Subjects with suspected sleep apnea syndrome. 4.Subjects who take medicines, herbs, and/or supplements that reducing blood sugar, inhibiting blood clotting and/or platelet aggregation. 5.Subjects who use pacemakers and/or defibrillators. 6.Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, and/or affected with infectious diseases requiring reports to the authorities. 7.Subjects with major surgical history relevant to the digestive system. 8.Subjects with unusually high and/or low blood pressure, abnormal physical data and/or abnormal hematological data. 9.Subjects with severe anemia. 10.Pre- or post-menopausal women complaining of obvious physical changes. 11.Subjects who are at risk of having allergic reactions to drugs and/or foods. 12.Subjects who cannot abstain from taking medicine and/or functional foods which would affect sleep and/or stress during this study. 13.Heavy smokers, alcohol addicts and/or subjects with disordered lifestyle. 14.Subjects whose lifestyle is expected to change. 15.Subjects who may be awakened at night by those who live together, etc. 16.Subjects who donated either 400 ml whole blood within 16 wks (women), 12 wks (men), 200 ml whole blood within 4 wks, or blood components within 2 wks, prior to this study. 17.Pregnant or lactating women or women who expect to be pregnant. 18.Subjects who currently participate in other clinical trials, or participated within the last 4 wks prior to this study. 19.Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.
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