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The study is an early feasibility study to measure individual patient clinical outcomes and effectiveness, evaluate the safety and function of the DUO Transcatheter Tricuspid Coaptation Valve System (DUO System).
Full description
Multi-center, prospective, non-randomized, investigational, and pre-market. Data collected in this clinical study will include safety and function of the investigational system as well as up to 5 year clinical outcomes.
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Interventional model
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15 participants in 1 patient group
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Central trial contact
Helen Scotch; Aubrey Dyer
Data sourced from clinicaltrials.gov
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