ACTRN12618000467235已完成4 期
Doxycycline as a cardioprotective agent in ST-elevation myocardial infarction: a pilot study addressing pre- reperfusion administration
Alfred Hospital0 个研究点目标入组 103 人开始时间: 2018年3月29日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 103
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •Consecutive men aged greater than 18 years and women aged greater than 55, or women less than 55 years and have no possibility of being pregnant; and
- •- Presenting within 12 hours of the onset of chest pain and with ECG findings of anterior or inferior ST-segment elevation or new left bundle branch block and for whom the clinical decision has been made to treat with PPCI; and
- •- Occlusion of the culprit related artery (TIMI grade 0 or TIMI grade 1) on coronary angiography, proximal and/or mid left anterior descending artery (LAD), or proximal dominant left circumflex (LCx) or dominant right coronary artery (RCA)
排除标准
- •Historical or Electrocardiograph (ECG) evidence of previous myocardial infarction; or
- •Patients with prior coronary artery bypass grafting (CABG); or
- •Previous revascularisation procedure where this procedure (PCI) was performed in the LAD/RCA; or
- •Known pre-existing left ventricular dysfunction; or
- •Known or suspected pregnancy; or
- •Patients presenting with cardiac arrest or cardiogenic shock; or
- •Patients undergoing rescue PCI for failed thrombolysis; or
- •Patients with left main coronary artery stenosis of such severity that after PCI of their culprit lesion (LAD/RCA) they are likely to require coronary artery bypass graft (CABG) within the time course of the study period (6 months).
- •Known allergy to tetracyclines;
- •Contraindications to CMR
研究者
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