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临床试验/NL-OMON48350
NL-OMON48350已完成不适用

Sample and method comparison with Minicare point-of-care device for cardiac troponin I assay at the emergency department. - Comparison of fingerstick versus venous sample for troponin I.

Viecuri Medisch Centrum voor Noord-Limburg0 个研究点目标入组 130 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
130

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 至 99(—)

入选标准

  • * Patients 18 years or older with chest pain suspected of ACS.
  • * STEMI patient who already underwent rescue PCI; inclusion post PCI.

排除标准

  • * Out of hospital cardiac arrest.
  • * Patients with sudden onset tachycardia and a frequence 110 bpm or higher,
  • (supraventricular or ventricular).
  • * Patients who are hemodynamically unstable or in which an acute non-coronary
  • diagnosis is suspected, e.g. pulmonary embolism, thoracic aortic dissection etc.
  • * Patients already admitted for the same set of symptoms at a previous
  • healthcare institution before being transferred to the participating clinical
  • * Patients not willing or not able to provide informed consent due to their
  • medical condition as judged by the physician

研究者

发起方
Viecuri Medisch Centrum voor Noord-Limburg

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