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临床试验/NL-OMON42138
NL-OMON42138已完成不适用

SAFETY AND FEASIBILITY OF INTRACORONARY HYPOTHERMIA IN ACUTE MYOCARDIAL INFARCTION (SINTAMI) - SINTAMI

Catharina-ziekenhuis0 个研究点目标入组 10 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
已完成
入组人数
10

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

  • Patients will be eligible for this study when they are admitted for acute ST elevation myocardial infarction with a total ST-segment deviation of more than 5 mm and presenting within 6 hours after onset of complaints.
  • Patients should have a TIMI 0, 1 or 2 flow in the infarction related artery.
  • If these patients are hemodynamically stable and in an acceptable clinical condition, informed consent will be asked to participate in this study.

排除标准

  • Age < 18 year
  • Cardiogenic shock or pre-shock
  • Poor clinical condition with concomitant inconvenience like repeated vomiting, severe chest pain or elsewise according to the judgement of the treating interventionalist.
  • Patients with previous myocardial infarction in the culprit area of with previous bypass surgery
  • Tortuous coronary arteries
  • Complex or long-lasting primary PCI expected
  • Severe concomitant disease or conditions with a life expectancy of less than one year
  • Inability to understand and give informed consent either in first instance on the table or in second instance on the coronary care unit.
  • Other known myocardial diseases, such as moderate or severe left ventricular hypertrophy or cardiomyopathy
  • Pregnancy
  • Mobitz II block, trifascicular block, or total AV block
  • Patients in whom no access to the coronary circulation can be obtained by the
  • femoral artery or in whom femoral access was problematic

研究者

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