Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Sacramento, California 95817


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.


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.



Primary Contact:

Principal Investigator
Jason Rogers, MD
University of California, Davis

Backup Contact:


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: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.

Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.