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Coherent Sine Burst Electroporation (CSE) Ablation System US IDE Study for Patients With Atrial Fibrillation
NCT06784466 · View on ClinicalTrials.gov ↗
Study Summary
To evaluate the safety and effectiveness of the Argá Medtech CSE Ablation System in the treatment of atrial fibrillation.
Conditions Studied
Interventions
- DEVICE Argá Medtech Coherent Sine-Burst Electroporation (CSE) Ablation System
Study Locations (20)
Ohio
- TriHealth Cincinnati — Cincinnati
- Cleveland Clinic — Cleveland
- Ohio Health Research and Innovation Institute — Columbus
Other
- AZorg Aalst — Aalst
- Jessa Ziekenhuis — Hasselt
- KBC Split — Split
Georgia
- Emory — Atlanta
- Northside Hospital — Atlanta
Texas
- Texas Cardiac Arrhythmia Research Foundation — Austin
- Methodist — San Antonio
Alabama
- Grandview — Birmingham
Arizona
- Banner University Med Ctr — Phoenix
Arkansas
- Arrhythmia Research Group — Jonesboro
California
- UCSD — San Diego
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 360 participants |
| Start Date | 2025-09-10 |
| Est. Completion | 2027-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06784466
The ClinicalTrials.gov registry entry for NCT06784466 describes a study currently listed as recruiting. It is categorized as NA, 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 360 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arga Medtech, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Atrial Fibrillation (AF) appearing as the primary indexed condition, and to 1 intervention — of which Argá Medtech Coherent Sine-Burst Electroporation (CSE) 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: NCT06784466 reports 20 study locations spanning 14 distinct geographic areas — top geographies include Ohio, Other, Georgia. 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 NCT06784466 about?
NCT06784466 is a clinical study titled "Coherent Sine Burst Electroporation (CSE) Ablation System US IDE Study for Patients With Atrial Fibrillation". To evaluate the safety and effectiveness of the Argá Medtech CSE Ablation System in the treatment of atrial fibrillation.
What is the current status of trial NCT06784466?
This trial is currently recruiting. It is a NA study. The enrollment target is 360 participants. The study started on 2025-09-10. Estimated completion is 2027-08.
What conditions does trial NCT06784466 study?
This clinical trial studies the following conditions: Atrial Fibrillation (AF), Paroxysmal AF, Persistant 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 NCT06784466?
The interventions under investigation include: Argá Medtech Coherent Sine-Burst Electroporation (CSE) Ablation System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06784466?
This trial is sponsored by Arga Medtech, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06784466 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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