Expired Study
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Sacramento, California 95817


Purpose:

Prospective, two academic center, non-randomized pilot, acute in-patient study correlating pre-operative imaging studies, intra-operative measurements and intra-operative balloon aortic valvuloplasty (BAV) in patients with degenerative aortic stenosis undergoing surgical aortic valve replacement (SAVR) to understand the requirements (device size and radial strength) of emerging percutaneous heart valve technologies in the treatment of aortic stenosis.


Criteria:

Inclusion Criteria: - Age 18 years or older - Any patient with severe, symptomatic calcific aortic stenosis (AS) referred for elective surgical aortic valve replacement. - Severe AS: aortic valve area (AVA) ≤ 1.0 cm2 - Symptoms: dyspnea on exertion, heart failure, angina or syncope believed to be secondary to AS Exclusion Criteria: - Emergent surgical aortic valve replacement. - Inability to undergo TTE or TEE intra-operatively. - Currently participating in another study that has not completed the primary endpoint or that clinically interferes with the current study endpoints.


NCT ID:

NCT00584116


Primary Contact:

Principal Investigator
Jason Rogers, MD
University of California, Davis


Backup Contact:

N/A


Location Contact:

Sacramento, California 95817
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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