TTVR STRONG Under Coverage With Evidence Development (CED) Study
Start Date
3/19/2025
Completion Date
12/31/2032
Summary
This Coverage with Evidence Development (CED) study measures the long-term health outcomes of patients with severe, symptomatic Tricuspid Regurgitation who received a Transcatheter Tricuspid Valve Replacement procedure using the EVOQUE system.
Detailed Description
This is a retrospective, non-randomized cohort study measuring 2-year effectiveness of the EVOQUE Transcatheter Tricuspid Valve Replacement (TTVR) system in the real-world. This study will retrospectively evaluate EVOQUE treated patients in the STS/ACC TVT Registry who have at least severe Tricuspid Regurgitation and can be deterministically linked with Medicare data. This group will be compared to Medicare eligible and EVOQUE eligible patients evaluated in a standard of care setting from a commercial claims database linked with electronic health records. We will evaluate the primary outcome measure in various subgroups. There will be continued access enrollment after the primary completion date.
Eligibility Criteria
Age Range: 65 years to No maximum
Interventions
EVOQUE
Conditions
Locations
Edwards Lifesciences
Irvine, California 92614
United States