NCT00764205Unknown不适用
Randomized Trial of Prehospital Troponin Assessment Using the i-STAT Blood Analyzer
Redmond Fire Department Medic One1 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2006年11月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 1,200
- 试验地点
- 1
- 主要终点
- Decrease door-to-reperfusion time for patients with non-STEMI's by measuring troponin levels prior to hospital arrival
研究概览
简要总结
This study randomizes patients seen by Redmond Medic One into a control arm and a study arm when they present with acute coronary syndrome and have non-contributory ECG's (i.e.non-STEMI). The control group is treated normally and delivered to the receiving hospital. The study group is treated normally as well, however troponin measurements are made using an i-STAT blood analyzer prior to hospital arrival. The results are presented to the receiving physician. Door-to-reperfusion time is monitored for both groups.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 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
- •Over years of age
- •ACS without ST-segment elevation
- •Patient being transported to one of two participating hospitals
排除标准
- •Less then 18 years of age.
- •Post cardiac arrest.
- •ACS with ST-segment elevation.
结局指标
主要结局
Decrease door-to-reperfusion time for patients with non-STEMI's by measuring troponin levels prior to hospital arrival
时间窗: 3-4 years
次要结局
未报告次要终点
研究者
研究点 (1)
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