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Pulmonary Vein Ablation of Atrial Fibrillation Using Magnetic Navigation: Single Ring Versus Circumferential Techniques

Pulmonary Vein Ablation With Magnetic Navigation in Patients With Therapy-refractory Symptomatic Atrial Fibrillation: Comparison of Single Ring and Circumferential Ablation Techniques

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01583075
Enrollment
80
Registered
2012-04-23
Start date
2009-12-31
Completion date
Unknown
Last updated
2012-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Vein Isolation, Ablation Time, Procedure Time, Freedom Form Atrial Fibrillation

Brief summary

The single-ring ablation method aims for isolation of the posterior LA wall including the pulmonary veins. If avoiding ablation on the posterior LA wall esophageal injury is unlikely. Aim of this prospective study was to evaluate the safety and efficacy of an RMN-guided single-ring ablation method as compared to standard RMN-guided circumferential PVA.

Interventions

Circumferential pulmonary vein ablation

PROCEDUREsingle ring pulmonary vein ablation

single ring pulmonary vein ablation

Sponsors

Stereotaxis
CollaboratorINDUSTRY
University Medical Center Goettingen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* drug refractory AF patients undergoing PVA

Exclusion criteria

* drug refractory AF patients undergoing repeat PVA

Design outcomes

Primary

MeasureTime frameDescription
Acute procedural successAfter the end of the ablation procedurenumber of PVs isolated at the end of the ablation procedure

Secondary

MeasureTime frameDescription
Long-term procedural success12 monthslong-term freedom from any AT/AF episodes

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026