JPRN-UMIN000033177已完成未知
Study for confirming body weight, body fat, visceral fat reducing effect by ingesting test food (dose setting test) - Study for confirming body weight, body fat, visceral fat reducing effect by ingesting test food (dose setting test)
CPCC Company Limited0 个研究点目标入组 40 人开始时间: 2019年7月6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
- 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 64years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Subjects who are given continuous treatment by taking medicines. 2)Subjects who constantly use oral medicines, functional foods and/or supplements having a possibility of affecting test results. 3) Those who have a weak gastrointestinal. 4) Subjects who have previous and/or current medical history of serious disease in heart, liver, kidney and/or digestive trucks. (5)Subjects who have previous and/or current medical history of serious disease in heart, liver, kidney and/or digestive trucks. (6)Subjects who excessive alcohol intake. (7)Subjects who have extremely irregular life rhythm, and subjects who have midnight work or irregular shift work. (8)Subjects who have previous medical history of drug and/or food allergy. (9)Subjects who are participating the other clinical tests of medicines or foods. Subjects who participated other clinical tests of medicines or foods within 4-weeks prior to the current study. Subjects who are planning to participate in other clinical tests of medicines or foods after agreeing with participating in this study. (10)Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. (11)Males who donated over 400mL blood within the last three month to the current study. (12) Females who donated over 400mL blood within the last four month to the current study. (13) Males who will be collected over 1200mL blood, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (14) Females who will be collected over 800mL blood, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (15) Subjects who are severely anemic, or who have been diagnosed with a severe anemia by the doctor (16)Others who have been determined ineligible by principal investigator or sub-investigator.
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