EICHORCondition: Aortic Stenosis · Aortic Stenosis, Severe · Sponsor: Edwards Lifesciences
Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
This study will assess the safety and effectiveness of the SAPIEN 3/SAPIEN 3 Ultra transcatheter heart valve (THV) in patients with a failing aortic bioprosthetic valve.
This description comes directly from the study's public registry record.
Edwards THV Clinical Affairs · (949) 250-2500 · THV_CT.gov@Edwards.com
Always discuss trial participation with your own doctor first.
| Banner University Medical Center | Phoenix, Arizona, United States | Recruiting |
| University of California Los Angeles | Los Angeles, California, United States | Recruiting |
| Sutter Medical Center | Sacramento, California, United States | Recruiting |
| Kaiser Permanente San Francisco | San Francisco, California, United States | Withdrawn |
| Stanford University Medical Center | Stanford, California, United States | Recruiting |
| UC Health Northern Colorado/Medical Center of the Rockies | Loveland, Colorado, United States | Recruiting |
| Hartford Hospital | Hartford, Connecticut, United States | Recruiting |
| JFK Medical Center/ Atlantic Clinical Research Collaborative | Atlantis, Florida, United States | Withdrawn |
| University of Florida, Gainesville | Gainesville, Florida, United States | Withdrawn |
| Emory University Hospital | Atlanta, Georgia, United States | Recruiting |
| Northwestern University Hospital | Chicago, Illinois, United States | Recruiting |
| Rush University Medical Center | Chicago, Illinois, United States | Recruiting |
+ 39 more locations — full list on the registry record.
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT03003299