JPRN-UMIN000029484已完成未知
A clinical study for evaluating of the effect of a complex food on postprandial serum triglyceride. - Clinical study for the effect on TG
Iryouhoujinsyadan Shoureikan Shinsapporo Seiryou Hospital0 个研究点目标入组 40 人开始时间: 2018年11月29日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 40
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 with hepatic, renal, cardiac or organ disorders or diabetes or other serious diseases. (2) Subjects with a surgical history of digestive system (except appendicectom). (3) Subjects with a history of a previous drug or food allergy. (4) Subjects currently under treatment with chronic diseases. (5) Subjects who are pregnant or intend to become pregnant during the study or are lactating. (6) Subjects who are lactose intolerant or sensitive to fatty diet to show gastrointestinal symptoms. (7) Subjects who take excessive alcohol (equivalent to 540 mL of Japanese sake or more) for 5 days or more per week. (8) Subjects who take drugs or supplements which claim the suppressive absorption of sugar or lipid or reduction of triglyceride, etc. (9) Subjects who participate in other clinical trial. (10) Subjects who have a history of feeling ill or unwell during or after blood drawing. (11) Subjects who have donated over 200 mL of blood within the last one month prior to this study or expect to donate the same during the study. (12) Subjects with extremely irregular dietary life (shift worker, night- shift worker, etc.) (13) Subjects who had excessive eating and/or drinking during 3 days prior to each screening or prior to intervention period I or II. (14) Subjects who fasted repeatedly during 3 days prior to each screening or prior to intervention period I or II. (15) Subject who had excessive exercise than usual during 3 days prior to each screening or prior to intervention period I or II. (16) Subjects judged as unsuitable for this study by the investigator for other reasons.
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