EFICAS: Carmat Total Artificial Heart as a Bridge to Transplant in Patients With Advanced Heart Failure
Study Details
Study Description
Brief Summary
The objective of this clinical investigation is to evaluate the efficacy and the safety of the Carmat Total Artificial Heart for the treatment of refractory advanced heart failure in transplant eligible patients.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
A selection committee (composed of two independent experts in the field of cardiovascular surgery/cardiology and of PIs) assess the subject eligibility based on clinical and anatomic criteria. Clinically eligible patients will be distributed into two cohorts depending on their anatomic compatibility with the device:
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cohort 1: patients that are anatomically compatible will receive the Carmat TAH ;
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cohort 2: patients that are not anatomically compatible will receive standard therapy
The efficacy and safety of the Carmat TAH will be assessed in cohort 1 and compared to a level of efficacy defined by the published data on the commercially available TAH; and adjusted for INTERMACS patient profile.
The clinical utility and the costs of Carmat TAH will be assessed by comparing the cohort of subject receiving the Carmat TAH to the cohort of patients treated by standard therapy
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Carmat TAH Subjects implanted with Carmat TAH |
Device: Carmat Total Artificial Heart
Heart Replacement Therapy
|
Outcome Measures
Primary Outcome Measures
- Survival free of disabling stroke at 180 days post-implant [180 days]
Success is defined as survival free of disabling stroke (Modified Rankin score >3) at 180 days after Carmat TAH implantation or transplanted if before 180 days.
Secondary Outcome Measures
- Overall survival [180 days - 1 year]
Survival post-implant; Survival post-transplantation (Kaplan-Meier)
- General Health Status change [180 days - 1 and 2 years]
Measured with the EuroQol EQ-5D-5L questionnaire, health-related quality of life consisting of five dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) each of which can take one of five responses (EQ-5D-5L). The responses record five levels of severity (1:no problems; 2:slight problems; 3:moderate problems 4:severe problems; 5:extreme problems) within a particular EQ-5D dimension.
- Change in functional status measured by the Six Minutes Walk Test [180 days - 1 and 2 years]
The 6-min walk test is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes. The 6-minute walk distance provides a measure for integrated global response of multiple cardiopulmonary and musculoskeletal systems involved in exercise.
- Change in functional status [180 days - 1 and 2 years]
New York Heart Association (NYHA) functional classification (regression scale I, II, III, IV)
- Adverse Events [180 days - 1 and 2 years]
Adverse Event Rates will be captured per the INTERMACS definitions
- Hospital re-admissions rate [180 days - 1 and 2 years]
Rate of unplanned re-admissions to the hospital
- Healthcare costs [180 days - 1 and 2 years]
The healthcare resources used to treat the patient during the two-year period, including those related to selection, those related to waiting for transplantation (whatever the therapeutic strategy), to transplantation, post-transplant management and any adverse event
- Quality Adjusted Life Years [180 days - 1 and 2 years]
The Quality Adjusted Life Years, evaluated during the two-year period, values the health outcomes in a single measure by combining both quality of life (evaluated by EuroQol EQ-5D-5L) and lenght of life.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patient 18 years or older
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Patient in the waiting list for heart transplant or temporarily contraindicated for heart transplant
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Inotrope dependent* or cardiac Index (CI) < 2.2 L/min/m2 if inotropes are contra-indicated (heart failure due to restrictive or constrictive physiology).
- Inotrope dependence needs to be confirmed by failed weaning or justified in medical records.
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On Optimal Medical Management as judged by the investigator based on current Heart Failure practice guidelines (ESC/HAS)
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Eligible to biventricular Mechanical Circulatory Support according to one of the following category:
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Biventricular failure with at least two of the following hemodynamic/ echocardiographic measurements implying right heart failure:
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RVEF ≤ 30%
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RVSWI ≤ 0.25 mmHg*L/m2
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TAPSE ≤ 14mm
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RV-to-LV end-diastolic diameter ratio > 0.72
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CVP > 15 mmHg
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CVP-to-PCWP ratio > 0.63
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PAP index <2
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Tricuspid insufficiency grade 4
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Treatment-refractory recurrent and sustained ventricular tachycardia or ventricular fibrillation in the presence of untreatable arrhythmogenic pathologic substrate.
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Heart failure due to restrictive or constrictive physiology (e.g., hypertrophic cardiomyopathy, cardiac amyloidosis / senile or other infiltrative heart disease)
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Anatomic compatibility confirmed using 3D imaging (CT-scan) and by the screening committee
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Patient's affiliation to health care insurance
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Patient has signed the informed consent.
Exclusion Criteria:
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Absolute contra-indication for heart transplant
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Existence of any ongoing non-temporary mechanical circulatory support
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Existence of any ongoing peripheral mechanical circulatory support such as ECMO, Impella (all types), IABP with a support duration > 21 days
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Patient intubated and unconscious; or intubated and not awake
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Known intolerance to anticoagulant or antiplatelet therapies or known Heparin Induced Thrombocytopenia.
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Coagulopathy defined by platelets < 100G/l or INR ≥ 1.5 not due to anticoagulant therapy.
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Known thrombophilia (Antithrombin III, protein C or S deficiency) or any recurrent venous thromboembolic events requiring long term curative oral anticoagulation.
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Cerebrovascular accident < 3 months or symptomatic (Rankin score >1; Glasgow score <
- or a known > 80% carotid stenosis.
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Known abdominal or thoracic aortic aneurysm > 5 cm that has not been treated.
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Severe end-organ dysfunction as per the following criteria:
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Total bilirubin > 45 µmol/l (2.65 mg/dl) or cirrhosis evidenced by ultrasound, IRM and positive biopsy
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GFR < 40ml/min/1.73m2 (with no hemodialysis)
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History of severe Chronic Obstructive Pulmonary Disease or severe restrictive lung disease with FEV1/FVC <0.7, or FEV1<50% predicted.
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Recent active blood stream infection confirmed by a positive hemoculture within 48 hours.
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Documented amyloid light-chain (AL amyloidosis).
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Hemodynamically significant peripheral vascular disease assessed by clinical exam.
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Illness, other than heart disease, that would limit survival to less than 2 years.
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Irreversible cognitive dysfunction, psycho-cognitive disabilities, psycho-social issues or psychiatric disease, likely to impair compliance with the study protocol and TAH management that in the opinion of the investigator could interfere with the ability to manage the therapy (i.e. non-compliance to heart failure therapy, uncontrolled diabetes, mental health issue, etc.).
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Pregnancy or breast feeding (woman in childbearing age will have to show negative pregnancy test).
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Patient is currently enrolled or has participated in the last 30 days in another therapeutic or interventional clinical study that is likely to confound the study results or affect the study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hôpital Louis Pradel, | Bron | France | 69500 | |
| 2 | Centre Hospitalier Régional Universitaire | Lille | France | 59000 | |
| 3 | Groupe Hospitalier Pitié-Salpêtrière, | Paris | France | 75013 | |
| 4 | Hôpital Pontchaillou | Rennes | France | 35033 | |
| 5 | Hôpital de Rangueil | Toulouse | France | 31059 |
Sponsors and Collaborators
- Carmat SA
Investigators
- Study Director: Piet Jansen, MD, Carmat SA
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CAR2019-FR