Found 12 matching trials
Impella®-Supported PCI in High-Risk Patients With Complex Coronary Artery Disease and Reduced Left Ventricular Function NA The purpose of this study is to assess if using the Impella® CP (or Impella...
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Active Not Recruiting
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University of Alabama
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Protect II, A Prospective, Multicenter Randomized Controlled Trial PHASE3 The IMPELLA® 2.5 System will be superior to Intra Aortic Balloon Pump in pr...
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University of Alabama
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MINI-AMI: Minimizing Infarct Size With Impella 2.5 Following PCI for Acute Myocardial Infarction NA A prospective, randomized, controlled multi-site feasibility trial to asses...
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Multiple Locations
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Comparison of Standard Treatment Versus Standard Treatment Plus Extracorporeal Life Support (ECLS) in Myocardial Infarction Complicated With Cardiogenic Shock PHASE4 Cardiogenic shock is currently the main cause of death after myocardial inf...
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Brest University Hospital
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Cardiogenic Shock Working Group Registry N/A The Cardiogenic Shock Working Group is a multicenter registry where we coll...
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Cleveland Clinic Florida
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Percutaneous Hemodynamic Support With Impella 2.5 During Scar-related Ventricular Tachycardia Ablation NA The purpose of this research study is to evaluate the safety and feasibilit...
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Mount Sinai School of Medicine
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Investigating the Role of Impella 2.5 System in Acutely Decompensated Chronic Heart Failure Patients NA The primary objective of this study is to assess safety and feasibility of ...
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Multiple Locations
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Efficacy Study of LV Assist Device to Treat Patients With Cardiogenic Shock (ISAR-SHOCK) PHASE4 The purpose of this study is to evaluate the efficacy and safety of a left ...
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Deutsches Herzzentrum Muenchen
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Impella Real-World Surveillance of Patients Using Sodium Bicarbonate N/A The population enrolled in this study are all subjects who received an Impe...
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University of Alabama
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PROTECT I, A Prospective Feasibility Trial Investigating the Use of IMPELLA RECOVER LP 2.5 System in Patients Undergoing High Risk PCI PHASE2 The objective of this feasibility study is to demonstrate that the device i...
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