Beating Heart Mitral Valve Repair With the HARPOON™ System
← catalyst calendarNCT04375332 · readout in 487 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
25actual
Sites
9
Country
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2020-12-16 | actual | When the study began enrolling |
| Primary completion | 2027-12-20 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-12-20 | estimated | The whole study's end, after follow-up |
| First posted | 2020-05-05 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-19 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Mitral Regurgitation
Intervention
- Device: HARPOON™ Beating Heart Mitral Valve Repair System
Primary outcome
what the primary-completion date above is the date OFChange in NYHA classification from Baseline to 5 years
measured Baseline compared to 1 and 5 years
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