JPRN-UMIN000045751已完成未知
Effect of Daily Ingestion of Test food on Improving Minor Health Complaints: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study - Effect of Daily Ingestion of Test food on Improving Minor Health Complaints
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 50
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 50years-old（—）
- 性别
- Female
入选标准
- 未提供
排除标准
- •1.Subjects who are under physician's advice, treatment, and/or medication for schizophrenia, depression, mania, neurological disorders, sleep disorders and/or chronic fatigue syndrome. 2.Subjects with suspected depression. 3.Subjects with implantable electronic medical devices. 4.Subjects with major surgical history relevant to the digestive system such as gastrectomy, gastrorrhaphy, enterectomy, etc. 5.Subjects with unusually high and/or low blood pressure and/or abnormal body measurement data and/or abnormal hematological data. 6.Subjects whose BMI is <16 kg/m2 or >=30 kg/m2 7.Subjects with severe anemia. 8.Subjects who are at risk of having allergic reactions to 28 food allergic substances and/or materials of test food. 9.Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 10.Pre- or post-menopausal women complaining of obvious physical changes. 11.Pregnant, lactating women or women who expect to be pregnant during this study. 12.Subjects who regularly take which contains materials of test foods. 13.Subjects who regularly take medicine, functional foods, and/or supplements which would affect sleep and/or stress. 14.Subjects who plan to travel abroad during this study. 15.Subjects whose lifestyle changed within a year prior to the current study. 16.Subjects whose lifestyle is expected to change. 17.Subjects who donated either 400 ml whole blood within 16 weeks, 200 ml whole blood within 4 weeks, or blood components within 2 weeks, prior to the current study, or subjects who do not agree not to donate blood during this study. 18.Subjects who currently participate in other clinical trials, or participated within the last 4 weeks prior to the current study, or intend to participate in order clinical trials after obtaining consent to participate in 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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