Supporting Patients Undergoing HIgh-Risk PCI Using a High-Flow PErcutaneous Left Ventricular Support Device (SHIELD II)
DescriptionProspective, randomized, multi-center, open-label trial of the HeartMate PHP at up to 120 sites in the US and Europe. Control device will be any Abiomed Impella device approved for use in high-risk PCI. This clinical investigation is divided into two phases, a feasibility phase and a pivotal phase. - Feasibility Phase: Includes 75 roll-in and 120 randomized subjects registered under the CIP versions 1-4 at 48 sites in the United States (U.S.) prior to January 30, 2017 - Pivotal Phase: Includes subjects to be registered under the current or later version of the CIP at up to 120 sites in the U.S. and Europe Non-randomized Roll-in Cohort: Up to 480 subjects with the HeartMate PHP; each operator must treat a minimum of 1 and up to 2 subjects with the HeartMate PHP first before becoming qualified to randomize subjects Randomized Cohort: A minimum of 473 and a maximum of 716 subjects will be randomized in a 2:1 ratio to the HeartMate PHP and Impella.
Inclusion and Exclusion Criteria
- Inclusion Criteria:
- At least 18 years of age
- Patient is undergoing elective or urgent high risk PCI procedure and is hemodynamically stable
- Patient is indicated for a revascularization of at least one de novo or restenotic lesion in a native coronary vessel or bypass graft
- A heart team, including a cardiac surgeon, has determined high risk PCI is an acceptable therapeutic option
- Written, signed, and dated informed consent Imaging Inclusion Criteria: • The presence of complex coronary artery disease (CAD) makes hemodynamic instability resulting from repeat episodes of reversible myocardial ischemia during PCI likely. Complex CAD is defined as an ejection fraction of <50% AND at least one of the following:
- intervention of the last patent coronary conduit, OR
- intervention of an unprotected left main artery, OR
- intervention on patient presenting with triple vessel disease defined as at least one significant stenosis (at least 50% diameter stenosis on visual assessment) in all three major epicardial territories Exclusion Criteria:
- Emergency PCI
- Any prior coronary revascularization within the last 6 months
- Hemodynamically unstable MI with elevated cardiac biomarker (creatinine kinase-MB (CK-MB) or troponin >1X upper limit of normal (ULN)) and no evidence of at least 1 consecutive CKMB or troponin value trending downward from previous value (at least 4 hours apart) OR ST Elevation MI (STEMI) within 72 hours prior to the index procedure regardless of the level of cardiac biomarker
- Cardiac arrest within 24 hours of procedure requiring cardiopulmonary resuscitation (CPR) or defibrillation
- Hemodynamic support with the HeartMate PHP post-PCI is anticipated.
- Staged PCI is planned within 90 days following device removal.
- Cardiogenic shock (SBP <90 mmHg for >1 hour with either cool clammy skin OR oliguria OR altered sensorium AND cardiac index <2.2 L/min/m2)
- History of aortic valve replacement or repair
- Documented presence of aortic stenosis (orifice area of 1.5cm2 or less)
- Severe peripheral vascular disease that will preclude the use of a 14F access sheath, which is required for the insertion of the HeartMate PHP catheter
- Known abnormalities of the aorta that would preclude surgery, including aneurysms and significant tortuosity or calcifications
- Subject is on hemodialysis.
- Liver dysfunction with elevation of liver enzymes and bilirubin levels to ≥ 3X ULN or Internationalized Normalized Ratio (INR) ≥2 or lactate dehydrogenase (LDH) > 2.5X ULN
- Uncorrectable abnormal coagulation parameters (platelet count ≤75000/mm3 or INR ≥2.0 or fibrinogen ≤1.5 g/l)
- Active systemic infection requiring treatment with antibiotics
- Stroke or transient ischemic attack (TIA) within 6 months of procedure
- Any allergy or intolerance to ionic and nonionic contrast media, anticoagulants, or antiplatelet therapy drugs that cannot be adequately premedicated
- Subject is pregnant (For a female subject of childbearing potential, a pregnancy test must be performed within 14 days (≤14 days) prior to the index procedure per site standard test).
- Participation in another clinical study of an investigational drug or device that has not met its primary endpoint
- Presence of other anatomic or comorbid conditions, or other medical, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with followup requirements, or impact the scientific soundness of the clinical investigation results Imaging Exclusion Criteria:
- Mural thrombus in the left ventricle
- Moderate to severe aortic insufficiency by echocardiographic assessment
Please contact the trial administrator to learn more about where you can participate in this trial. Please use the contact form on the right side.