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ADVENT Post Approval Study
NCT06431815 · View on ClinicalTrials.gov ↗
Study Summary
The ADVENT Post Approval Study (PAS) is a prospective, global, multicenter, observational study.
Conditions Studied
Interventions
- DEVICE FARAPULSE™ Pulsed Field Ablation System
Study Locations (20)
Florida
- Florida Heart Rhythm Specialists, PLLC — Fort Lauderdale
- Baptist Medical Center — Jacksonville
- Mount Sinai Medical Center — Miami Beach
- Tallahassee Memorial Hospital — Tallahassee
- AdventHealth Tampa — Tampa
New York
- New York Hospital Queens — Flushing
- Columbia University Medical Center — New York
- Northwell Health — New York
- Montefiore Medical Center — The Bronx
Alabama
- Mobile Infirmary Medical Center — Mobile
Arizona
- Scottsdale Healthcare - Shea — Scottsdale
California
- Alta Bates Summit Medical Center — Oakland
District of Columbia
- Washington Hospital Center — Washington D.C.
Georgia
- Memorial Health University Medical Center — Savannah
Louisiana
- Ochsner Clinic Foundation — New Orleans
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 228 participants |
| Start Date | 2024-09-25 |
| Est. Completion | 2029-10 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06431815
The ClinicalTrials.gov registry entry for NCT06431815 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 228 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Scientific Corporation, which has 120 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Paroxysmal Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention — of which FARAPULSE™ Pulsed Field Ablation System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06431815 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Florida, New York, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06431815 about?
NCT06431815 is a clinical study titled "ADVENT Post Approval Study". The ADVENT Post Approval Study (PAS) is a prospective, global, multicenter, observational study.
What is the current status of trial NCT06431815?
This trial is currently active not recruiting. The enrollment target is 228 participants. The study started on 2024-09-25. Estimated completion is 2029-10.
What conditions does trial NCT06431815 study?
This clinical trial studies the following conditions: Paroxysmal Atrial Fibrillation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06431815?
The interventions under investigation include: FARAPULSE™ Pulsed Field Ablation System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06431815?
This trial is sponsored by Boston Scientific Corporation, which has 120 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06431815 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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