NL-OMON55210招募中不适用
A multicentre randomized controlled trial to improve the AccUracy of Referrals to the emerGency departmEnt of patieNts with chesT pain by using the modified HEART score in Emergency Medical Transport(URGENT 2.0) - Improving the accuracy of referrals of patients with chest pain.
Viecuri Medisch Centrum voor Noord-Limburg0 个研究点目标入组 852 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
- 招募中
- 发起方
- 入组人数
- 852
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
- •- Age >= 18 years.
- •- Chest pain or other complaints suspect of ACS for at least 2 hours where the
- •GP or emergency medical personnel are in need of further diagnostics or risk
- •stratification to come to a decision of referral.
- •- Patients, who have been informed of the nature of the study, agree to its
- •provisions and have provided written informed consent.
排除标准
- •-- Electrocardiographic ST-segment elevation/High suspicion of STE-ACS.
- •- Suspicion of an acute non-coronary diagnosis e.g. pulmonary embolism,
- •thoracic aortic dissection or other life-threatening disease.
- •- Patients presenting cardiogenic shock, defined as: systolic blood pressure
- •<90mmHg and heart rate >100 and peripheral oxygen saturation <90% (without
- •oxygen administration)
- •- Patients presenting with sudden onset heart rhythm disorders and second or
- •third degree atrioventricular block.
- •- Patients with confirmed ACS, PCI or CABG <30 days prior to inclusion.
- •- Impaired consciousness defined as an EMV <8.
- •- Severe shortness of breath.
- •- Patients with known end-stage renal disease (dialysis and/or MDRD < 30
- •- Patients with known cognitive impairment.
- •- Communication issues with patient/language barrier.
- •- Patients already participating in an interventional cardiology or
- •cardiovascular trial.
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