JPRN-UMIN000017870已完成未知
A study for evaluating the effect of the intake of an indigestible dextrin-containing beverage on postprandial hyperglycemia : randomized, placebo-controlled, double blind cross-over trial - A study for evaluating the effect of the intake of indigestible dextrin-containing beverage on postprandial hyperglycemia
TTC Co.,Ltd.0 个研究点目标入组 60 人开始时间: 2015年6月12日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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 64years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Subjects who routinely use food containing of indigestible dextrin (2) Subjects routinely taking medicine or health food which may influence glucose metabolism (3) Subjects who are under medication or having a history of serious diseases for which medication was required (4) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (5) Subjects having possibilities for emerging allergy related to the study (6) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (7) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study (8) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (9) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (10) Subjects judged as unsuitable for the study by the investigator for other reasons
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