Lead Evaluation for Defibrillation and Reliability Post Approval Study
← catalyst calendarNCT07005232 · readout ≤ 2,234 d
Sponsored by Medtronic (industry) · MDT — their whole pipeline →.
Phase
—
Status
Enrolling by invitation
Study type
Observational
Enrollment
2,000estimated
Sites
73
Countries
Austria, Canada, France +4
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 | 2026-01-07 | actual | When the study began enrolling |
| Primary completion | Sep 2032 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Sep 2032 | estimated | The whole study's end, after follow-up |
| First posted | 2025-06-05 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-03 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Tachyarrhythmia
Intervention
- Device: defibrillation lead
Primary outcome
what the primary-completion date above is the date OFComplication Survival Rate
measured 5 years
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