跳至主要内容
临床试验/JPRN-UMIN000018813
JPRN-UMIN000018813已完成未知

a study on SDI-DLB concerning to diagnose DLB and assess benefit for Donepezil : Study 2 - SDI-DLB: diagnose DLB and assess benefit for Donepezil(Study 2)

Promedico Co., Ltd.0 个研究点目标入组 30 人开始时间: 2015年8月28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
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
60years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • •1)dozed antidementia drugs except Donepezil within 12 weeks before informed consent 2)bed ridden 3)with severe impairment of visual acuity, auditory sensor and/or communication 4)with neurological degenerative disease except for DLBV criteria, schizophrenia, bipolar disorder and major depression 5)with delirium due to abuse of alcohol, drugs, metabolic toxicity and inflammation 6)inadequate decided by principal investigator 7)with hypersensitivity to components of Donepezil or piperidine derivative 8)dozed investigational drug within 12 weeks before informed consent

研究者

发起方
Promedico Co., Ltd.

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