Cerebral Protection in Transcatheter Aortic Valve Replacement

Completed · Not applicable

Conditions studied: Severe Symptomatic Calcified Native Aortic Valve Stenosis

In brief

The Sentinel System will be a safe and effective method for capturing and removing embolic material (thrombus/debris) during transcatheter aortic valve replacement in order to reduce the ischemic burden in the cerebral anterior circulation.

Key facts

Study ID

NCT02214277

Run by

Claret Medical

People needed

363

Starts

2014-09-01

Expected to finish

2016-06-01

Last updated by the study team

2018-05-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Approved indications for commercially available Edwards SAPIEN Transcatheter Heart Valve, model 9000TFX or SAPIEN XT, model 9300TFX meeting one of the three sub-criteria below:
• SAPIEN
• transfemoral delivery in subjects with severe symptomatic calcified native aortic valve stenosis without severe aortic insufficiency and with ejection fraction >20% who have been examined by a heart team including an experienced cardiac surgeon and a cardiologist and found to either be:
• inoperable and in whom existing co-morbidities would not preclude the expected benefit from correction of the aortic stenosis; or
• be operative candidates for aortic valve replacement but who have a Society of Thoracic Surgeons predicted operative risk score >8% or are judged by the heart team to be at a 15% risk of mortality for surgical aortic valve replacement.
• or
• transapical delivery in subjects with severe symptomatic calcified native aortic valve stenosis without severe aortic insufficiency and with ejection fraction > 20% who have been examined by a heart team including an experienced cardiac surgeon and a cardiologist and found to be operative candidates for aortic valve replacement but who have a Society of Thoracic Surgeons operative risk score 8% or are judged by the heart team to be at a 15% risk of mortality for surgical aortic valve replacement.
• SAPIEN XT (Transfemoral or Transapical only)
• in patients with symptomatic heart disease due to severe native calcific aortic stenosis (aortic valve area ≤ 1.0 cm2 or aortic valve area index ≤ 0.6 cm2/m2, a mean aortic valve gradient of ≥ 40 mmHg, or a peak aortic-jet velocity of ≥ 4.0 m/s), and with native anatomy appropriate for the 23, 26, or 29 mm valve system, who are judged by a heart team, including a cardiac surgeon, to be at high or greater risk for open surgical therapy (i.e., Society of Thoracic Surgeons operative risk score ≥8% or at a ≥15% risk of mortality at 30 days).
• Compatible left common carotid artery (6.5 - 10 mm) and brachiocephalic artery (9 - 15 mm) diameters without significant stenosis (> 70%) as determined by Multi-Slice Computed Tomography (MSCT) scan or equivalent imaging modality
• The subject and the treating physician agree that the subject will return for all required post-procedure follow-up visit
• The subject or the subject's legal representative has been informed of the nature of the trial, agrees to its provisions and has provided written informed consent as approved by the IRB of the respective clinical site

You may not qualify if…

• General
• Vasculature in the right extremity precluding 6Fr sheath radial or brachial access
• Inadequate circulation to the right extremity as evidenced by signs of artery occlusion (modified Allen's test) or absence of radial/brachial pulse
• Hemodialysis shunt, graft, or arterio-venous fistula involving the upper extremity vasculature
• Evidence of an acute myocardial infarction ≤ 1 month before the intended treatment
• Aortic valve is a congenital unicuspid or bicuspid valve; or is non-calcified
• Mixed aortic valve disease (aortic stenosis and aortic regurgitation with predominant aortic regurgitation >3+)
• Any therapeutic invasive cardiac procedure resulting in a permanent implant that is performed within 30 days of the index procedure (unless part of planned strategy for treatment of concomitant coronary artery disease)
• Pre-existing prosthetic heart valve in any position, prosthetic ring, or severe (greater than 3+) mitral insufficiency
• Blood dyscrasias as defined: Leukopenia, acute anemia, thrombocytopenia, history of bleeding diathesis or coagulopathy
• Hemodynamic instability requiring inotropic support or mechanical heart assistance.
• Need for emergency surgery for any reason
• Hypertrophic cardiomyopathy with or without obstruction
• Severe ventricular dysfunction with LVEF ≤20%
• Echocardiographic evidence of intracardiac or aortic mass, thrombus, or vegetation
• Symptomatic or asymptomatic severe occlusive carotid disease requiring concomitant CEA/stenting
• Subject has undergone carotid stenting or carotid endarterectomy within the previous 6 weeks
• Active peptic ulcer or upper GI bleeding within the prior 3 months
• A known hypersensitivity or contraindication to aspirin, heparin, ticlopidine, or clopidogrel, or sensitivity to contrast media, which cannot be adequately pre-medicated
• Recent (within 6 months) CVA or a TIA
• Renal insufficiency (creatinine > 3.0 mg/dL or GFR < 30) and/or renal replacement therapy at the time of screening
• Life expectancy < 12 months due to non-cardiac co-morbid conditions
• Subjects in whom anti-platelet and/or anticoagulant therapy is contraindicated, or who will refuse transfusion
• Subjects who have active bacterial endocarditis or other active infections
• Currently participating in an investigational drug or another device study

Where it is running

• Cedars-Sinai Medical Center — Los Angeles, California, United States
• Washington Hospital Center — Washington D.C., District of Columbia, United States
• Morton Plant Hospital — Clearwater, Florida, United States
• Emory University Hospital — Atlanta, Georgia, United States
• Henry Ford Hospital — Detroit, Michigan, United States
• Barnes-Jewish Hospital — St Louis, Missouri, United States
• Columbia University Medical Center — New York, New York, United States
• Icahn School of Medicine at Mount Sinai — New York, New York, United States
• Weill Cornell Medical Center — New York, New York, United States
• Cleveland Clinic Foundation — Cleveland, Ohio, United States
• Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States
• UT Houston / Memorial Hermann — Houston, Texas, United States
• UVA Advanced Cardiac Valve Center — Charlottesville, Virginia, United States
• UW Medical Center — Seattle, Washington, United States
• Herzzentrum Leipzig - Universitatsklinik — Leipzig, Germany

Full record on ClinicalTrials.gov

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