跳至主要内容
临床试验/NL-OMON48009
NL-OMON48009已完成不适用

The safety and efficacy of implementing the PreHEART decision support tool by the Emergency Medical Service for patients with undifferentiated chest pain: a prospective randomized open blinded end-point study (PreHeart-3 study) - PreHEART 3: The best care in the right place

niversitair Medisch Centrum Groningen0 个研究点目标入组 5,150 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
入组人数
5,150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Patients above 17years old,
  • Patients with undifferentiated chest discomfort
  • Ability to communicate in Dutch or English

排除标准

  • Communication barrier (e.g. language, understanding),
  • ST-segment elevation myocardial infarction (electrocardiogram on scene is
  • standard workup),
  • Any obvious etiology for the symptoms requiring direct treatment (e.g. trauma),
  • Being previously evaluated by EMS for the same complaint (already considered
  • for participation)
  • High clinical suspicion of a life-threating condition (e.g. sudden death
  • survivor, hypothermia, shock, aortic dissection, hypoxia or intoxication),
  • Cognitive impairment,
  • End-stage renal disease,
  • Inability or unwillingness to provide informed consent,
  • Not registered with a GP (huisarts).

研究者

相似试验