JPRN-UMIN000041013已完成未知
A Study on the Effect of Food Containing Plant Extract on Postprandial GLP-1 -A Randomized, Double-blind, Placebo-controlled, Cross-over Study- - A Study on the Effect of Food Containing Plant Extract on Postprandial GLP-1
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 12
研究概览
简要总结
Statistically significant difference was confirmed in the primary outcome.
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 have a chronic disease and regularly use medications. (2)Subjects who can't stop using supplements and/or functional foods (including Food for Specified Health Uses or Foods with Function Claims) during test periods. (3) Subjects who can't stop drinking from 2 days before each measurement. (4)Subjects who have declared allergic reaction to ingredients contained in test foods or loading foods. (5) Subjects who contract or are under treatment for diseases (e.g., diabetes, liver disease, kidney disease, heart disease, respiratory disease, endocrine disease and/or metabolic disease). (6)Subjects who have a history and/or a surgical history of digestive disease affecting digestion and absorption. (7)Subjects who are judged unsuitable for the current study by the screening tests. (8)Subjects who are diagnosed as anemic by the screening tests and unsuitable for frequent blood sampling. (9) Subjects who have had diarrhea within the last one week prior to the screening tests. (10)Subjects who have donated over 200 mL of blood and/or blood components within the last one month or over 400 mL of blood and/or blood components within the last three months prior to the current study. (11)Subjects who are under treatment for or have a history of drug addiction and/or alcoholism. (12) Subjects who are shiftworker and/or midnight-shift worker. (13) Subjects who are planning to participate in other clinical studies during test periods and/or had participated in other clinical studies within the last one month prior to the current study. (14) Subjects who are planning to become pregnant after informed consent, pregnant or lactating. (15) Subjects who are judged unsuitable for the current study by the investigator for other reasons.
研究者
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