跳至主要内容
临床试验/JPRN-UMIN000010813
JPRN-UMIN000010813招募中未知

A randamized, double-blind, placebo-controlled, parallel group study to evaluate the efficacy and safety of oral administration of probiotic LKM512 in individuals with pre-arteriosclerosis - Effects of probiotics LKM512 in individuals with pre-arteriosclerosis: double-blind, placebo-controlled parallel group study

Kyodo Milk Industry Co. Ltd.0 个研究点目标入组 30 人开始时间: 2013年5月27日最近更新:

试验速览

阶段
未知
状态
招募中
入组人数
30

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)Subjects who are undergoing dyslipidemia treatment (2)Subjects who take medicine that influencea value of cholesterol (3)Seriouse subjects who have complications with cardiac disease, hepatic disease, and/or renal disease (4)Subjects who was enrolled in other trails within three month. (5)Inappropriate cases evaluated by doctors

研究者

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