Evaluation of TAVR Using the NAVITOR Valve in a Global Investigation
NAACTIVE_NOT_RECRUITING
Evaluation of TAVR using the NAVITOR valve in a Global Investigation.
Study details:
The VANTAGE clinical trial will evaluate the safety and effectiveness of the Navitor valve in patients with severe, symptomatic aortic stenosis who are at intermediate or low risk of surgical mortality. This trial will also evaluate the safety and effectiveness of the Navitor valve in a valve-in-valve application.
Eligibility criteria
Researchers look for people who fit a certain description, called eligibility criteria. See if you qualify.
Inclusion criteria
- Subject who is judged by a Heart Team, including a cardiac surgeon, to be appropriate for transcatheter heart valve intervention therapy, and is deemed to be at intermediate or low risk for open surgical aortic valve replacement (i.e., heart team estimates risk of surgical mortality < 7% at 30 days, considering the Society of Thoracic Surgeons (STS) risk score, overall clinical status, and other clinical co-morbidities unmeasured by the risk calculator).
- New York Heart Association (NYHA) Functional Classification of II, III, or IV.
- Degenerative aortic valve stenosis with echo-derived criteria, defined as: aortic valve area (AVA) of ≤ 1.0 cm2 (or indexed EOA ≤ 0.6 cm2/m2) AND either mean gradient ≥ 40 mmHg or peak jet velocity ≥ 4.0 m/s or doppler velocity index (DVI) ≤ 0.25. The echocardiogram supporting the qualifying AVA baseline measurement must be performed within 90 days prior to informed consent.
- Aortic annulus diameter of 19-30 mm and ascending aorta diameter of 26-44 mm for the specified valve size listed in the IFU, as measured by CT (systolic phase) conducted within 12 months prior to informed consent.
Exclusion criteria
- Life expectancy is less than 2 years in the opinion of the Investigator.
- Evidence of an acute myocardial infarction [defined as ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) with acute ischemia symptoms and troponin elevation] within 30 days prior to index procedure.
- Untreated clinically significant coronary artery disease requiring revascularization.
- Any percutaneous coronary or peripheral interventional procedure performed within 30 days prior (except pacemaker or implantable cardioverter defibrillator (ICD) implant) to index procedure or planned within 30 days following the index procedure.
- Blood dyscrasias as defined: leukopenia (WBC < 3000 mm3), acute anemia (Hb < 9 g/dL), thrombocytopenia (platelet count < 50,000 cells/mm³); history of bleeding diathesis or coagulopathy
- Active peptic ulcer or upper GI bleeding within 3 months prior to index procedure that would preclude anticoagulation
- Recent (within 6 months prior to index procedure date) cerebrovascular accident (CVA) or a transient ischemic attack (TIA)
- Renal insufficiency (creatinine > 3.0 mg/dL or eGFR < 30 ml/min/1.73m2) and/ or end stage renal disease requiring chronic dialysis
- Hostile chest or conditions or complications from prior surgery that would make the subject be considered high surgical risk (i.e., mediastinitis, radiation damage, abnormal chest wall, porcelain aorta, adhesion of aorta or internal mammary artery to sternum, etc.)
- Significant frailty as determined by the heart team (after objective assessment of frailty parameters) that would indicate high or extreme surgical risk
- Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation 3-4+)
- Aortic valve is a congenital unicuspid or congenital bicuspid valve as verified by echocardiography or CT
- Severe ventricular dysfunction with LVEF < 30% as measured by resting echocardiogram
- Pre-existing prosthetic heart valve or other implant (such as prosthetic ring or transcatheter edge-to-edge repair (TEER) clip) in any valve position (Note: Subjects with a bioprosthetic aortic valve may be included in the ViV cohort.)
- Severe circumferential mitral annular calcification (MAC) which is continuous with calcium in the left ventricular outflow tract (LVOT)
- Severe (greater than or equal to 3+) mitral regurgitation or severe mitral stenosis with pulmonary compromise
- Minimum access vessel diameter of < 5.0 mm for small FlexNav Delivery System and < 5.5 mm for large FlexNav Delivery System
- Eccentricity ratio of the annulus < 0.73
Eligibility
Age eligible for study : NA
Healthy volunteers accepted : No
Gender eligible for study: ALL
Things to know
Study dates
Study start:
Primary completion:
Study completion finish:
Study type
TREATMENT
Phase
- NA
Study ID
NCT04788888
Intervention or treatment
DEVICE: Navitor Transcatheter Aortic Valve and FlexNav Delivery System
Conditions
- Symptomatic Severe Aortic Stenosis
You may be eligible to participate in this trial based on your search. Check eligibility by answering some questions.
Research sites nearby
Closest Location:
The Alfred Hospital
Select from list below to view details:
The Alfred Hospital
Melbourne, Australia
St. Andrew's Hospital
Adelaide, Australia
Fiona Stanley Hospital
Murdoch, Australia
Macquirie University Hopsital
Ryde, Australia
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Who is running the clinical trial?
AMD
Abbott Medical Devices
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
| Participant Group/Arm | Intervention/Treatment |
|---|---|
EXPERIMENTAL: Primary Analysis Cohort
| Device: Navitor Transcatheter Aortic valve and FlexNav Delivery system |
What is the study measuring?
Primary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of a composite of all-cause mortality or fatal stroke/stroke with disability at 12 months (Primary Safety Endpoint) | A composite of all-cause mortality or fatal stroke/stroke with disability at 12 months post index Navitor implantation procedure per the Valve Academic Research Consortium (VARC) 3 event definitions | 12 months post index procedure |
| The proportion of subjects who have moderate or greater paravalvular leak at 30 days (Primary Effectiveness Endpoint) | Moderate or greater paravalvular leak at 30 days | 30 days post index procedure |
Secondary Outcome
| Measure | Description | Time Frame |
|---|---|---|
| Transvalvular gradient | Mean change in mean transvalvular gradient between baseline and 12 months | 12 months post index procedure |
| Effective orifice area | Mean change in effective orifice area between baseline and 12 months | 12 months post index procedure |
| KCCQ quality of life score | Mean change in KCCQ quality of life score between baseline and 12 months | 12 months post index procedure |
Are you running this trial?If you're a clinic or sponsor, you can claim this study.
References
Clinical Trials Gov: Evaluation of TAVR Using the NAVITOR Valve in a Global InvestigationOther trials to consider
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