ADVENT Trial Long Term Outcomes Evaluating Atrial Fibrillation Progression Study
← catalyst calendarSponsored by Boston Scientific Corporation (industry) · BSX — their whole pipeline →.
Phase
—
Status
Completed
Study type
Observational
Enrollment
364actual
Sites
25
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 | 2024-10-31 | actual | When the study began enrolling |
| Primary completion | 2025-12-08 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-12-08 | actual | The whole study's end, after follow-up |
| First posted | 2024-07-30 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-03-02 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Paroxysmal Atrial Fibrillation
Primary outcome
what the primary-completion date above is the date OFChronic success in ADVENT Trial treated subjects compared between treatment groups.
measured 90 day-3 years
Publications
- PMID 41652117 — linked by the registry
Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.
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