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临床试验/JPRN-UMIN000004597
JPRN-UMIN000004597已完成未知

Safety and efficacy of Edaravone[Nichiiko] in patients with acute noncardiogenic brain embolism - Safety and efficacy of Edaravone[Nichiiko] in patients with acute noncardiogenic brain embolism

Takeshi Yamada0 个研究点目标入组 20 人开始时间: 2010年12月3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 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • the investigators must ensure that all subjects being considered to meet the following exclusion criteria or conditions: 1)difficult lifesaving in a coma 2)serum creatinine >= 1.5 mg/dL 3)history of allergy to Edaravone 4)cardiogenic brain embolism 5)hemorrhagic infarction, epidural hemorrhage, intracerebral hemorrhage, intraventricular hemorrhage 6)transient ischemic attack 7)patients are less than 3 months from the last onset in case of reappearance 8)mRS before the onset >= grade 2 9)patients who are administrated the excluded drugs between onset and investigational drug administration 10)patients who are recieved the excluded therapies between onset and investigational drug administration 11)A serious heart disease(e.g heart failure) or hepatic disease(e.g cirrhosis hepatis) to need hospitalization treatment 12)Patients have cancer 13)Patients who are or may be pregnant, who are lactating 14)recent (past 3 months) participation in other clinical trial for investigational agent,the investigator determines this trial participation inadequate

研究者

发起方
Takeshi Yamada

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