EUCTR2010-023394-19-NL进行中（未招募）1 期
Early Beta blocker Administration before reperfusion in patients with ST-Elevation Myocardial Infarction who are planned to undergo primary PCI - Early-ßAMI
Maatschap Cardiologie Isala0 个研究点目标入组 601 人开始时间: 2010年11月17日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 601
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients = 18 years of age with symptoms of acute ST-elevation myocardial infarction of more than 30 min but less than 12 hours and on the ECG ST-segment elevation of >= 0.1 mV in two adjacent limb electrocardiograph (ECG) leads and >= 0.2 mV in two adjacent precordial ECG leads or new left bundle branch block (LBBB).
- •Verbal followed by written informed consents.
- •PCI-center located within 90 minutes
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 301
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 300
排除标准
- •Severe Hypotension (systolic blood pressure < 100 mmHg)
- •Cardiogenic shock (severe dyspnoea, hypotension and oxygen saturation <92%, systolic blood pressure < 100 mmHg and heartrate > 110/min)
- •Known with asthma
- •Severe bradycardia at sinusrythm (< 60 bpm)
- •PR interval >240 ms or second- and/or third degree atrio-ventricular (AV) block
- •History of previous myocardial infarction
- •Killip class III-IV
- •Pacemaker/implantable cardioverter defibrillator (ICD)
- •Unable to provide informed consent
- •Patient is pregnant or breastfeeding
研究者
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