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临床试验/NCT00673036
NCT00673036Unknown不适用

French Registry of Acute Coronary Syndrome With or Without ST Elevation

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 3,750 人开始时间: 2005年10月最近更新:
适应症

试验速览

阶段
不适用
入组人数
3,750
试验地点
1
主要终点
All causes mortality at each follow-up period

研究概览

简要总结

The Fast-MI registry was designed to evaluate the "real world" management of patients with acute myocardial infarction (MI), and to assess their in-hospital, medium and long-term outcomes

详细描述

Primary objectives : compare survival following the admission to a USIC according to the terms of care

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

入选标准

  • admission within the 48 hours after the occurence of acute myocardial infarction (AMI)
  • written informed consent for the DNA and serum databank

排除标准

  • AMI occured within the 48 hours after therapeutic intervention (bypass, coronary angioplasty or other chirurgical intervention)
  • diagnostic of AMI not confirmed

结局指标

主要结局

All causes mortality at each follow-up period

时间窗: 6 months, each year

次要结局

  • Cardiovascular mortality(6 month, each year)
  • Pharmacogenetic and cardiovascular genetic studies associated to clinical outcomes(6 month each year)
  • validation of guidelines across the country(6 month, each year)
  • Serum databank for evaluation of biomarkers in MI(6 month each year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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