JPRN-UMIN000006607已完成2 期
G-CSF employing neuroprotection study for ischemic stroke -Phase 2 clinical trial-(GENESIS-2) - G-CSF employing neuroprotection study for ischemic stroke -Phase 2 clinical trial-(GENESIS-2)
Tokai University, School of Medicine, Division of Neurology, Department of Internal Medicine.0 个研究点目标入组 100 人开始时间: 2011年12月1日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 100
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
- 45years-old 至 85years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Splenomegaly or splenic lesions on echo. 2.Leukocytosis more than 15000/mm3 3.Past history of G-CSF treatment. 4.Plan for percutaneous angiography or bypass operations. 5.Difficult to perform MRI. 6.Past histries of symptomatic intracranial hemorrhage, bleeding tendency or coagulating disorders. 7.Hyper reactivity to G-CSF. 8.Congestive heart failure or uncontrollable angina. 9.Thrombocytopenia(less than 140000/mm3) 10.Liver dysfunction(AST(GOT),ALT(GPT) more than 100 IU/L) 11.Renal dysfunction (creatinine 1.5mg/dl and more) 12.Difficult to continue this trial due to social problems, etc. 13.Join other clinical trials. 14.Inappropriate to enroll in this trial by the judgment of the doctor.
研究者
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