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临床试验/ACTRN12618000467235
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

发起方
Alfred Hospital

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