跳至主要内容
临床试验/JPRN-UMIN000024460
JPRN-UMIN000024460已完成未知

A clinical study for evaluating safety of excessive consumption -Non-blind, safety verification study taking 5 times dose of test food "ECM-E" in healthy adults. - A clinical study for evaluating safety of excessive consumption -Non-blind, safety verification study taking 5 times dose of test food "ECM-E" in healthy adults.

Adaptgen Pharmaceutical Co., Ltd.0 个研究点目标入组 20 人开始时间: 2016年11月1日最近更新:
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 45years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • The following exclusion criteria apply to subjects. 1)A person with the disease in gastrointestinal tract, liver, kidney, heart and circulatory system which have an influence on the absorption, distribution, metabolism and excretion of test food 2)A person with a major surgery history in the gastrointestinal tract sites such as gastrectomy, stomach and intestines suture, the intestinal resection (however, polypectomy, the appendectomy are excluded) 3)A person with a history of cerebrovascular disorder (the asymptomatic lacunar infarct is excluded) 4)A person with tattoo which has an influence on the study because of its size or range 5)A person with hypersensitivity or idiosyncrasy, such as food allergy 6)A person who is suspected to have alcohol or drug dependence 7)A person who has participated in other clinical trials within 84 days from giving an informed consent 8)A person who donated 400 ml of blood within 84 days, 200 ml within 28 days, or a blood component (plasma or platelets) within 14 days from giving an informed consent 9)A person who hopes pregnancy or who cannot prevent conception during the study 10)A nursing or pregnant woman 11)A person who is engaged in night duty

研究者

相似试验

A clinical study for evaluating safety of excessive... | 临床试验