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临床试验/JPRN-UMIN000017133
JPRN-UMIN000017133已完成未知

Assessment of Safety of a Supplement Containing Mushroom Chitosan in Case of Excess Ingestion - Safety of a Supplement Containing Mushroom Chitosan

TES Holdings Co., Ltd.0 个研究点目标入组 24 人开始时间: 2015年4月14日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
24

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 59years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • [1]Individuals using or will use medical products [2]Individuals who had a habit to ingest health-promoting foods [3]Individuals who are or are posslibly, or are lactating [4]Individuals who excessively take alcohol [5]Individuals who have symptoms of allergy to the test product [6]Individuals who participate in other clinical studies [7]Individuals who have a history of serious hepatopathy, kidney damage, heart disease and hematological disease [8]Individuals with serious anemia [9]Individuals who had been administrated contrast material (ex. barium) in the past 2 months or will be administrated during the test period

研究者

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