JPRN-UMIN000045750已完成未知
Effect of Daily Ingestion of the Barley on Improving Minor Health Complaints: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Comparison Study - Beneficial Effect of the Barley on Improving Minor Health Complaints
适应症
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
- 30years-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 schizophrenia, depression, mania, neurological disorders, and/or sleep disorders. 2.Subjects with gastrointestinal disorders. 3.Subjects who take antihypertensive agents, immunosuppressive drugs, and/or indomethacin. 4.Subjects who used antibiotics within 12 wks, prior to the current study. 5.Subjects with implantable electronic medical devices. 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 such as gastrectomy, gastrorrhaphy, enterectomy, etc. 8.Subjects with unusually high and/or low blood pressure 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 or foods especially based on wheat. 12.Subjects who regularly take medicine, functional foods, and/or supplements which contains GABA. 13.Subjects who regularly use gastrointestinal drugs. 14.Subjects with defecation frequency less than 2 times per week. 15.Subjects who repeat constipation and diarrhea. 16.Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 17.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 the current study. 18.Pregnant or lactating women or women who expect to be pregnant during this study. 19.Subjects who currently participate in other clinical trials, or participated within the last 4 wks prior to the current study. 20.Subjects whose lifestyle is expected to change significantly. 21.Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.
研究者
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