NL-OMON27238已完成不适用
The PreHEART3 study
none0 个研究点目标入组 5,150 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 5,150
研究概览
简要总结
PreHEART development and validation study has been submitted
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Adults with undifferentiated chest pain.
排除标准
- •Communication barrier (e.g. language, understanding)
- •ST-segment elevation (electrocardiogram on scene is standard workup)
- •Any obvious etiology for the symptoms requiring direct treatment (e.g. trauma)
- •Being previously evaluated by ambulance personnel 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)
- •COVID suspicion
研究者
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