跳至主要内容
临床试验/NL-OMON24829
NL-OMON24829招募中不适用

IMPella versus IABP REduces mortality in STEMI patients treated with primary PCI IN SEVERE and deep cardiogenic SHOCK.<br>An international multicenter, randomized trial of the Impella* cVAD (left ventricular assist) device versus Intra Aortic Balloon Counter Pulsation (IABP) therapy for acute ST-elevation myocardial infarction patients treated with primary PCI in severe and deep cardiogenic shock.

Academic Medical Center, Departement of Cardiology0 个研究点目标入组 48 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
招募中
发起方
入组人数
48

研究概览

简要总结

/A

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Delay between onset of chest pain and PCI ≤ 24-72 hours;
  • 2. Cardiogenic shock defined as: systolic blood pressure ≤ 90 mmHg for > 30 minutes or the need for supportive measures to maintain a systolic blood pressure ≥ 90 mmHg;

排除标准

  • 1. Severe aorta-iliac arterial disease impeding placement of either devices;
  • 2. Known severe cardiac aortic valvular disease;

研究者

发起方
Academic Medical Center, Departement of Cardiology

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