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Edwards EVOQUE Eos MISCEND Study

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NCT02718001 · readout in 620 d

Sponsored by Edwards Lifesciences (industry) · EW — their whole pipeline →.

Phase
Not applicable
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
123estimated
Sites
19
Countries
Canada, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2015-02-06actualWhen the study began enrolling
Primary completion2028-04-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2033-04-30estimatedThe whole study's end, after follow-up
First posted2016-03-24estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Mitral Valve Regurgitation (Degenerative or Functional)

Intervention

  • Device: Edwards EVOQUE Eos Mitral Valve Replacement System — also filed as CardiAQ-Edwards™ Transcatheter Mitral Valve (TMV), Edwards FORTIS™ Transcatheter Mitral Valve (TMV), Transcatheter Mitral Valve Replacement (TMVR), Edwards EVOQUE Transcatheter Mitral Valve Replacement System

Primary outcome

what the primary-completion date above is the date OF
Composite of major adverse events
measured 30 days

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