JPRN-UMIN000038956已完成未知
A Study on the Effect of Plant Extract on Postprandial Blood Glucose and Serum Triglyceride -A Randomized, Double-blind, Placebo-controlled, Cross-over Study- - A Study on the Effect of Plant Extract on Postprandial Blood Glucose and Serum Triglyceride
适应症
试验速览
- 阶段
- 未知
- 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 65years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Subjects whose fasting blood glucose level is 126 mg/dL and over or two-hour blood glucose level after 75 g glucose loading is 200 mg/dL and over and/or who have been diagnosed with diabetes. (2) Subjects whose fasting serum triglyceride level is 45 mg/dL or less and 150 mg/dL or over, or casual serum triglyceride level is 650 mg/dL and over. (3) Subjects who contract or are under treatment for serious diseases (e.g., diabetes, liver disease, kidney disease, digestive system disease, heart disease, respiratory disease, peripheral vascular disorder, etc.). (4) Subjects who use oral medication affecting blood glucose or lipid metabolism. (5) Subjects who constantly use supplements and/or functional foods (including Food for Specified Health Uses, Foods with Functional Claims) affecting blood glucose or lipid metabolism. (6) Subjects with abnormal parameters in liver and/or kidney function. (7) Subjects who have a history of digestive disease surgery. (8) Subjects with a disease that may have an influence on this study currently under treatment. (9) Subjects who have declared an allergic reaction to test foods, or loading foods. (10) Subjects with anemia or who have difficulty with self blood collection. (11) Subjects who play high intensity sports and/or are on a diet. (12) Subjects with irregular life patterns. (13) Subjects who use medicines (including OTC and/or prescribed medications) continuously. (14) Subjects who drink excessive alcohol, or who can't stop drinking from one day before each measurement. (15) Subjects who are planning to become pregnant after informed consent for the current study or are pregnant or lactating. (16) Subjects who are planning to participate in other clinical studies. (17) Subjects who are judged as unsuitable for the study by the investigator for other reasons.
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