Kerckhoff Klinik
Bad Nauheim, Hesse, 61231, Germany
NCT Number: NCT02697006
The purpose of this study is to collect prospective safety and performance information for the i-COR® device using synchronized cardiac assist in the setting of combined heart-lung failure or in high risk percutaneous intervention procedures in catheterization lab.
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Notify Me18 year–85 year
All sexes
Observational
Bad Nauheim, Hesse, 61231, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients in cardiogenic shock in the setting of acute myocardial infarction
or
Patients undergoing high risk coronary revascularization procedures (e.g., multi-vessel disease, left main, or last patent conduit interventions) in the catheterization lab.
Cardiogenic shock is defined as
Written consent of the patient or the legal caregiver
-
Exclusion criteria
The i-cor Synchronized Cardiac Assist Device delivers pulsatile cardiac assist synchronized to the ECG during diastole and provides enhanced oxygenation through a membrane oxygenator.
Time frame: 30 days
Acute safety defined as rates of device and procedure related serious adverse events up to 30 days post-intervention.
Time frame: 24 hours
Technical success (defined as the ability to successfully deliver the i-COR® SYNCHRONIZED CARDIAC ASSIST device without serious adverse events).
Time frame: 7 days
Device performance success (defined as the ability to establish synchronized pulsatile cardiac assist, enhance cardiac function and improve tissue oxygenation) assessed immediately post-procedure (acute) and serially as the device remains in place and provides cardiac support over time in each patient.
Xenios AG
Industry
Synchronized Cardiac Assist for Cardiogenic Shock. The SynCor Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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