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临床试验/ACTRN12610000053022
ACTRN12610000053022已完成未知

In patients presenting to the emergency department with potential acute coroanry syndrome (ACS) is there a difference in the change in troponin (absolute and rate) and a traditional mulitmarker approach with risk stratification tools in excluding significant coronary artery disease?

Queensland Emergency Medicine Research Foundation0 个研究点目标入组 1,000 人开始时间: 2010年1月18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
1,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Inclusion criteria include all patients who present to the ED with at least 5 minutes of chest pain suggestive of ACS. In accord with American Heart Association (AHA) guidelines, these will include the presence of acute chest, epigastric, neck, jaw or arm pain or discomfort or pressure or breathlessness without apparent non-cardiac source. More general/atypical symptoms (such as fatigue, nausea, vomiting, sweating and faintness) will not be used as inclusion criteria.
  • Patients who have chest discomfort and in whom the attending staff consider it necessary to perform an electrocardiogram (ECG) for the assessment of possible ACS will be enrolled.

排除标准

  • Patients under the age of 18 years old
  • Unable or unwilling to consent
  • Patients for whom follow-up will not be possible either due to lack of contact address or because they will be overseas.

研究者

发起方
Queensland Emergency Medicine Research Foundation

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