JPRN-UMIN000012031已完成3 期
Placebo-controlled, double-blind, crossover clinical trial for the effect of single intake of soybean processed food rich in beta-conglycinin on postprandial hyperlipidemia - Effect of beta-conglycinin-rich soybean on postprandial hyperlipidemia
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 20
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 60years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Subjects who are under medication for chronic ailments. 2)Subjects with serious diseases and infections. 3)Subjects with clinical history of gastrointestinal surgery. 4)Subjects with frequent complaints of post-menopausal symptoms. 5)Subjects with unusually high and/or low blood pressure, or with abnormal hematological data. 6)Subjects with serious anemia. 7)Subjects with a history of allergy to medicine and food, especially soybean. 8)Subjects routinely on supplementation which would affect the lipid metabolism. 9)Heavy smokers and alcohol addicts, or subjects with irregular lifestyle. 10)Subjects who donate 400ml whole blood within 12 weeks or who donate plasma or platelets within 4 weeks prior to supplementation. 11)Subjects who are pregnant or under lactation, or ones who would be expected to be pregnant during the study. 12)Subjects who participate in other clinical trials within the last one month prior to the current clinical trial. 13)Subjects who are not eligible due to physician's judgment
研究者
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