跳至主要内容
临床试验/JPRN-UMIN000042647
JPRN-UMIN000042647已完成未知

A pharmacokinetics study of catechins - A pharmacokinetics study of green tea catechins after ingestion of green tea beverage

Central Research Institute, ITO EN, Ltd.0 个研究点目标入组 20 人开始时间: 2020年12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
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 40years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • (1)Subjects who are with treatment at the time of Advance inspection. (2)Subjects who have severe anemia. (3)Subjects whose blood test values are outside of the reference range at the time of Advance inspection. However this is not applicable to the subjects who are deemed to be able to participate in the test by the investigator. (4)Subjects who are with allergy to the study foods or meals during the hospital stay. (5)Subjects who are with current or past medical history of gastrointestinal disease, cardiovascular disease, nephritis and others. Subjects who are with severe mental disorder. (6) Subjects who are not negative for syphilis, HBs antigen, HCV antibody or HIV antigen/antibody test at the time of Advance inspection. (7)Subjects who cannot stop smoking during the hospital stay. (8)Subjects who took the OTC (including the oriental medicines), the Foods with health claims (Foods for specified health uses and others), the health foods, the supplements and others regularly within the past 1 month at the time of Advance inspection. (9)Subjects who have potential to change the lifestyle in the test period. (10) Subjects who donated 200mL of blood within the past 1 month or 400mL of blood within the past 3 months at the time of Advance inspection. (11)Subjects who are attending other studies or attended other studies within the past 3 months. (12)Subjects who are judged to be unsuitable for the test by the investigator.

研究者

发起方
Central Research Institute, ITO EN, Ltd.

相似试验