JPRN-UMIN000040659已完成未知
A study for evaluating the effects of oral intake of dietary fiber complex on body fat and intestinal flora in human. - A study for evaluating the effects of oral intake of dietary fiber complex on body fat and intestinal flora in human.
IMEQRD Co., Ltd0 个研究点目标入组 50 人开始时间: 2020年6月5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
- 50
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.Those who are currently receiving any types of medicines and/or Chinese medical treatments (except for the medicines that are taken as needed). 2.Those who have or had a severe disease of the liver, heart, kidneys, gastrointestinal tract, respiratory system, endocrine, and metabolism 3.Those who are receiving nutrition therapy or physical therapy under a doctor's supervision. 4.Those who received gastrointestinal surgery (except appendectomy). 5.Those who have been routinely taking medicines, foods with health claim (foods for specified health use, in particular), health foods, or supplements that may affect the body fat and/or bowel movement. 6.Those who cannot abstain from taking health foods during the study period. 7.Those who have a current or previous history of drug and/or food allergies. 8.Smokers. 9.Heavy drinkers. 10.Those who have metals implanted in the body due to surgery etc. 11.Those who have a cardiac pacemaker or an implantable medical device placed in the body. 12.Those who have claustrophobia. 13.Those who work night shifts. 14.Those who are currently undergoing treatment for drug dependence or drug abuse or those who have a past medical history of either of them. 15.Those who are currently pregnant or breastfeeding or those who want to become pregnant during the study period. 16.Those who are currently participating in another clinical trial or those who took a test product and completed another clinical trial in a month. 17.Those who were determined by the principal investigator and the sub investigator to be unsuitable for participation in this clinical trial.
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