CorVad Myocardial Infarction Complicated with Cardiogenic Shock Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorShenzhen Core Medical Technology CO.,LTD.

About this trial

Cardiogenic shock a serious complication of a heart attack (myocardial infarction). Despite evaluation of several new treatments during the last decade, the mortality in patients with cardiogenic shock still exceeds 50%. An alternative to current management is restoration of the volume of blood pumped by the heart (cardiac output) using a ventricular assist device. In the acute setting this is difficult but can be done using the CorVad device which is a catheter-based, axial flow pump that pumps blood directly from the left ventricle into the circulation thereby restoring blood flow to the failing organs. The hypothesis of the current study is to reduce mortality and morbidity of patients with cardiogenic shock using the CorVad device. The study will be carried out as a randomized multicenter study where eligible patients will be randomized to receive conventional circulatory support or support with the CorVad device and inotropic support if needed. A total of 269 patients are planned

Eligibility criteria

Qualifiers

ST segment elevation myocardial infarction of less than 36 hours' duration, confirmed by new onset ST-segment elevation, or emergency angiography demonstrating acute occlusion of coronary artery, and

Left ventricular ejection fraction of less than 45% visually estimated or by wall motion score index >1,6.

Disqualifiers

Shock duration N24 hours

Other causes of shock; hypovolemia, sepsis, pulmonary embolism or anaphylaxis

Shock due to mechanical complication to myocardial infarction; papillary muscle rupture, rupture of the ventricular septum or rupture of ventricular free wall.

Severe aorta valve regurgitation/stenosis

Trial design

Treatments tested in this trial

  • Conventional circulatory support
  • CorVad

Treatment groups

269 Participants
are divided into 2 treatment groups