Feasibility Study on the FARAVIEW Technology
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Phase
Not applicable
Status
Completed
Study type
Interventional
Design
Na · None · Treatment
Enrollment
50actual
Sites
3
Countries
Czechia, Ireland, Spain
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 | 2024-04-03 | actual | When the study began enrolling |
| Primary completion | 2025-05-15 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-06-06 | actual | The whole study's end, after follow-up |
| First posted | 2023-12-18 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-09-17 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Atrial Fibrillation
- Paroxysmal Atrial Fibrillation
- Persistent Atrial Fibrillation
Intervention
- Device: Ablation Treatment
Primary outcomes
what the primary-completion date above is the date OFNumber of subjects with PVI success
measured At the end of the ablation procedure
Number of subjects with PWI success
measured At the end of the ablation procedure
Physician feedback on FARAVIEW technology of the RHYTHMIA mapping system by means of a questionnaire
measured At the end of the ablation procedure
umber of subjects presenting with PV or PW reconnections site's standard of care method. Procedural complications: device and/or procedure-related AEs.
measured At the end of the ablation procedure
Publications
- PMID 41919393 — linked by the registry
- PMID 41474406 — 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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