TranScatheter Aortic Valve RepLacement System US Feasibility Trial

Status unconfirmed · Phase 2

Conditions studied: Aortic Valve Stenosis

In brief

A study to assess the safety and effectiveness of the Direct Flow Medical aortic valve system. This is for people with severe aortic stenosis who are not well enough to undergo a surgical repair. The delivery of this device is done via the femoral artery.

Key facts

Study ID

NCT01932099

Run by

Direct Flow Medical, Inc.

People needed

30

Starts

2013-08-01

Expected to finish

2018-12-01

Last updated by the study team

2016-10-31

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The patient has severe senile degenerative aortic valve stenosis determined by resting or dobutamine stress echocardiogram and Doppler, or simultaneous pressure recordings at cardiac catheterization defined as: mean gradient >40 mmHg or peak jet velocity >4.0 m/s and an aortic valve area ≤0.8 cm2 or aortic valve area index ≤0.5 cm2/m2.
• The patient has moderate to severe symptoms from aortic valve stenosis (NYHA Functional Class ≥III).
• The patient must have a predicted risk of operative mortality or serious irreversible morbidity of >50% at 30 days, or be deemed not suitable for surgery for other reasons. This conclusion shall be based on consensus of one cardiologist and two cardiac surgeons at the investigational site after careful consideration of the patient's STS risk score and co-morbidities, and after at least one of the surgeons participating in the decision has personally examined the patient.
• The patient been informed of the nature of the study, agrees to its provisions, is willing to comply with protocol-specified follow-up evaluations and has provided written informed consent, approved by the appropriate IRB.

You may not qualify if…

• Left ventricular ejection fraction (LVEF) <20% determined by resting echocardiogram
• Patients with an acute MI within 30 days preceding the index procedure.
• Any percutaneous coronary or peripheral interventional procedure performed within 30 days prior to the study procedure
• Patients with impaired renal function (estimated Glomerular Filtration Rate [eGFR] <20cc/min, calculated from serum creatinine by the Cockcroft-Gault formula)
• Patients with a platelet count of <50,000 cells/mm³ or a WBC < 1000 cells/mm³ within 7 days prior to index procedure.
• Patients with a history of bleeding diathesis or coagulopathy or patients in whom anti-platelet and/or anticoagulant therapy is contraindicated, or who will refuse transfusion.
• Patients who have received any organ transplant or are on a waiting list for any organ transplant.
• Patients with known other medical illness (e.g. carcinomas, chronic liver disease, chronic renal disease or chronic end stage pulmonary disease) or known history of substance abuse that may cause non-compliance with the protocol, confound the data interpretation or is associated with a life expectancy of less than one year, or expectation that patient will not improve despite treatment of aortic stenosis.
• Patients with known hypersensitivity or contraindication to aspirin, heparin, clopidogrel/ticlopidine, and/or contrast sensitivity that cannot be adequately pre-medicated.
• Patients with a history of a stroke or transient ischemic attack (TIA) within the prior 6 months.
• Patients with an active gastrointestinal (GI) bleeding within the prior 6 months.
• Patients presenting with hemodynamic instability or cardiogenic shock defined by low cardiac output, vasopressor dependence, or mechanical hemodynamic support.
• Patients who have a planned treatment with any other investigational device or procedure during the study period, or who are currently participating in an investigational drug or another device trial
• Any planned surgical, percutaneous coronary or peripheral procedure to be performed prior to the 30 day follow-up from the TAVR procedure.
• Untreated clinically significant coronary artery disease requiring revascularization
• Trans-esophageal echocardiography (TEE) is contraindicated
• Active endocarditis or sepsis within 6 months prior to the study procedure
• Dementia (resulting in either inability to provide informed consent for the trial/procedure, prevents independent lifestyle outside of a chronic care facility, or will fundamentally complicate rehabilitation from the procedure or compliance with follow-up visits)
• Congenital bicuspid or unicuspid valve determined by echocardiography
• Prior aortic or mitral valve surgery or pre-existing prosthetic heart valve in any position
• Native valve annulus diameter is <19mm or >26mm determined by the screening CT scan
• Extreme asymmetrical calcification of the native aortic valve determined by the screening CT scan
• Echocardiographic evidence of intra-cardiac mass, thrombus, vegetation, or spontaneous echo contrast in the left atrium
• >3+ aortic regurgitation, mitral regurgitation or tricuspid regurgitation
• Moderate to severe mitral stenosis

Where it is running

• UC Davis Medical Center — Sacramento, California, United States
• Northwestern Memorial Hospital — Chicago, Illinois, United States
• Henry Ford Hospital — Detroit, Michigan, United States
• Washington University Hospital — St Louis, Missouri, United States
• Columbia Univ. Medical Center — New York, New York, United States
• Cleveland CLinic — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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