跳至主要内容
临床试验/NL-OMON34319
NL-OMON34319撤回不适用

The accuracy, feasibility and safety of Fractional Flow Reserve in patients with acute ST-elevation myocardial infarction - FFR in STEMI

niversitair Medisch Centrum Groningen0 个研究点目标入组 50 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
撤回
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - A diagnosis of a STEMI defined by 1/A diagnosis of acute MI defined by chest pain suggestive for myocardial ischemia for at least 30 minutes, with a time from onset of symptoms of less than 12 hours, before hospital admission, 2/ ECG with ST- segment deviation of more than 0.1 mV in 2 or more leads and 3/Positive cardiac troponin T >0.01 *g/l.
  • - Clinical indication for urgent PCI of the infarct related lesion as identified at coronary angiography
  • - Planned staged PCI for a lesion in a non-infarct related vessel
  • - Verbal followed by written informed consent
  • - 18 years or older

排除标准

  • - Presence of cardiogenic shock
  • - Implantation or planned implantation of an intra-aortic balloon pump
  • - Failed reperfusion of the infarct related vessel (>30% residual stenosis and less than TIMI 3 coronary flow)
  • - No staged PCI possible
  • - Need for coronary artery bypass grafting
  • - No suitable anatomy of the non-IRV (Left main stenosis of >50%, Diameter <2.5mm, Extremely tortuous or calcified coronary arteries, Chronic total occlusion, Collaterals visible, Previous CABG
  • - Contra-indications for adenosine intracoronary (Second or third degree AV block, Sick sinus syndrome, Asthma, Hypersensitivity to adenosine)
  • - Inability to provide informed consent

研究者

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