NCT02194153已完成不适用
Surveillance of Patients With Suspected Acute Myocardial Infarction That Receive Prehospital or Early Inhospital (Emergency Department) Thrombolysis With Metalyse ®
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 351
- 主要终点
- Pain relief
研究概览
简要总结
Obtaining data on efficacy (e.g. complete ST-segment resolution) depending on the time of treatment initiation and safety of prehospital and early hospital thrombolysis with Metalyse® in a real life setting outside clinical trials.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Metalyse
Metalyse weight-adjusted
干预措施: Metalyse weight-adjusted (Drug)
结局指标
主要结局
Pain relief
时间窗: 90 min, 120 min, up to 30 days after treatment initiation
yes/no question
Complete ST-segment resolution
时间窗: up to 30 days
Change in creatine kinase (CK)
时间窗: up to 24 hours
Change in creatine kinase-MB (CK-MB)
时间窗: up to 24 hours
Change in troponin
时间窗: up to 24 hours
次要结局
未报告次要终点
研究者
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