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Completed

NCT Number: NCT02697006

Synchronized Cardiac Assist for Cardiogenic Shock

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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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Kerckhoff Klinik

Bad Nauheim, Hesse, 61231, Germany

Who can participate

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

  • Systolic blood pressure < 90 mmHg for at least 30 min or
  • Inotropes are needed to maintain blood pressure > 90 mmHg or
  • Clinical signs of heart insufficiency with pulmonary congestion or
  • Signs of end organ hypoperfusion with at least one of the following criteria:
  • Altered mental status
  • cold, damp skin or extremities
  • oliguria (≤ 30 mL/h)
  • serum lactate > 2.0 mmol/L

Written consent of the patient or the legal caregiver

-

Exclusion criteria

  • Age > 85 years
  • Cardiac arrest out of hospital with return of spontaneous circulation (ROSC) > 10 min
  • Coma with fixed pupils not induced by drugs;
  • Mechanical causes for cardiogenic shock (ventricular septal defect of papillary muscle rupture)
  • Non-cardiogenic causes of shock (bradycardia, sepsis, hypovolemia, etc.)
  • Fever (Body temperature > 38.0 °C) or other evidence of sepsis
  • Onset of cardiogenic shock > 6 h before enrollment;
  • Lactate > 22 mmol/L;
  • Massive pulmonary embolism;
  • Severe peripheral arterial occlusive disease precluding insertion of femoral arterial or venous catheters
  • Previous known aortic regurgitation greater than grade II
  • Contra-indications for anticoagulation
  • Severe hemolysis of any cause
  • Patient is participating in an investigational drug or device study trial that has not reached the primary endpoint or that interferes with the current study endpoints.

Treatment and study plan

i-cor Synchronized Cardiac Assist Device

Device

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.

Primary outcomes

  1. Number of Participants With Device and Procedure Related Serious Adverse Events

    Time frame: 30 days

    Acute safety defined as rates of device and procedure related serious adverse events up to 30 days post-intervention.

  2. Number of Participants Treated With Technical Success of the Device

    Time frame: 24 hours

    Technical success (defined as the ability to successfully deliver the i-COR® SYNCHRONIZED CARDIAC ASSIST device without serious adverse events).

  3. Number of Participants With Device Performance Success

    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.

Sponsors and collaborators

Lead sponsor

Xenios AG

Industry

Collaborators

  • Avania

Registry information

Official study title

Synchronized Cardiac Assist for Cardiogenic Shock. The SynCor Trial

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Mar 2, 2016
Registry last updated
Sep 16, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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