JPRN-UMIN000026090已完成未知
A Study on the Effect of Food Containing Plant Extract on Postprandial B1ood Glucose -A Randomized, Double-blind, Placebo-controlled, Cross-over Study- - A Study on the Effect of Food Containing Plant Extract on Postprandial B1ood Glucose
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 48
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 whose fasting blood glucose level are 126 mg/dL and over, or 2-hour glucose value in a 75 g oral glucose tolerance test are 200 mg/dL and over. (2)Subjects who use oral medications affecting blood glucose. (3)Subjects who can't stop using supplements and/or functional foods(including Food for Specified Health Uses or Foods with Function Claims) affecting blood glucose during test periods. (4)Subjects who have declared allergic reaction to test foods or ingredients contained in loading foods. (5)Subjects who are diagnosed as diabetes based on the results of screening test. (6)Subjects who contract, are under treatment for or have a history of serious diseases(e.g., diabetes, kidney disease, liver disease, and heart disease), thyroid gland disease, adrenal gland disease, and/or metabolic disorder. (7)Subjects who have a chronic disease and use medications continuously. (8)Subjects who have a history of digestive disease affecting digestion and absorption. (9)Subjects who are judged as unsuitable for the current study based on the results of screening test. (10)Subjects who are diagnosed as anemic and not suitable for frequent collection of blood. (11)Subjects who have had diarrhea within the last one week prior to the screening test. (12)Subjects who have donated over 200 mL of blood and/or blood components within the last one month prior to the current study or over 400 mL of blood and/or blood components within the last three months prior to the current study. (13)Subjects who are under treatment for or have a history of drug addiction and/or alcoholism. (14)Subjects who are planning to participate in other clinical studies. (15)Subjects who are planning to become pregnant after informed consent for the current study, are pregnant or lactating. (16)Subjects who are judged as unsuitable for the current study by the investigator for other reasons.
研究者
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