SVC-isolation in Redo-AF Ablation With Isolated PV

NCT ID: NCT07112716

Last Updated: 2025-08-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-01

Study Completion Date

2027-07-01

Brief Summary

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Atrial fibrillation is the most common arrhythmia in the population and is often caused by arrhythmogenic foci located in the pulmonary veins. For this reason, the first attempt in atrial fibrillation catheter ablation procedures is to isolate these structures (the procedure is called indeed "pulmonary vein isolation"), which results in abolishment of arrhythmia recurrence in up to 85% of patients at short and mid-term follow-up. However, a subset of patients experience an atrial tachyarrhytmia recurrence and a second catheter ablation procedure has to be performed. If pulmary vein isolation is proven to be durable, other arrhythmogenic foci could be implicated in arrhythmia recurrence. Among extra-pulmonary vein foci, superior vena cava has been described as the most frequently involved in atrial fibrillation initiation. Therefore, its ablation could result in improved freedom from atrial fibrillation episodes during follow-up. In the present study, we sought to evaluate the safety and effectiveness of empirical superior vena cava isolation in terms of arrhythmia-free survival in patients with paroxysmal atrial fibrillation recurrence despite durable pulmonary vein isolation.

Detailed Description

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Atrial fibrillation (AF) is the most frequent arrhythmia in the general population (1), with an expected doubling in prevalence within 2060 (2). Since the late 1990s (3), pulmonary vein isolation (PVI) has become a cornerstone in drug refractory AF treatment, and more recently has emerged a first line therapy in paroxysmal AF patients (4) due to its proven superiority to antiarrhythmic drugs in achieving arrhythmia-free survival (5).

PVI is a safe and effective procedure in the vast majority of patients with paroxysmal AF, with high AF-free survival at mid- and long-term follow-up. In case of AF recurrence, repeat ablation of pulmonary vein reconnections demonstrated superior outcomes compared to the use of anti-arrhythmic drugs in both paroxysmal and persistent AF (6). Nevertheless, a subset of patients with AF recurrence results to be "PVI non-responder", with arrhythmia recurrence despite durable ablation results (7). How to manage these patients is still a matter of debate, with different additional lesion sets proposed so far (8).

Non-PVI triggers have been implicated in AF initiation, with superior vena cava (SVC) being the most common of them (9,10). Empirical SVC isolation has been attempted in some observational as well as randomized study (11-14), but definitive conclusion could not be drawn due to lack of statistical power as well as variable eligibility criteria (first vs repeat procedure, paroxysmal vs persistent AF) and ablation sets (15).

In the present study, we sought to evaluate the safety and effectiveness of empirical SVC isolation in terms of arrhythmia-free survival in patients with paroxysmal AF recurrence despite durable PVI.

Conditions

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Paroxysmal AF

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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SVC isolation group

Empirical superior vena cava isolation

Group Type ACTIVE_COMPARATOR

Empirical superior vena cava isolation

Intervention Type PROCEDURE

Empirical superior vena cava isolation with radiofrequency ablation

Control arm

No empirical superior vena cava isolation

Group Type SHAM_COMPARATOR

Ablation without empirical superior vena cava isolation

Intervention Type PROCEDURE

No ablation or ablation of other arrhythmic foci wuthout empirical superior vena cava isolation

Interventions

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Empirical superior vena cava isolation

Empirical superior vena cava isolation with radiofrequency ablation

Intervention Type PROCEDURE

Ablation without empirical superior vena cava isolation

No ablation or ablation of other arrhythmic foci wuthout empirical superior vena cava isolation

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Age \> 18 years.
2. Confirmed diagnosis of recurrent paroxysmal AF
3. Previous transcatheter PVI-only procedure for AF.
4. Evidence of persistently isolated pulmonary veins at repeat procedure.
5. Signed informed consent.

Exclusion Criteria

* Age \< 18 years.
* Pregnancy.
* Concomitant investigation treatments.
* Medical, geographical and social factors that make study participation impractical, and inability to give written informed consent. Patient's refusal to participate in the study.
* Lesions other than PVI performed during first procedure
* Persistent AF at recurrence.
* Evidence of pulmonary vein reconnection at repeat procedure.
* Any additional lesion performed beyond SVC isolation during repeat procedure (in the empirical SVC isolation group only).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centro Medico Teknon

OTHER

Sponsor Role lead

Responsible Party

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Antonio Berruezo, MD, PhD

MD, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Antonio Berruezo, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Teknon Medical Centre

Locations

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Heart Institute, Teknon Medical Centre

Barcelona, Barcelona, Spain

Site Status

Countries

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Spain

Central Contacts

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Antonio Berruezo, MD, PhD

Role: CONTACT

93 290 62 51 ext. + 34

Diego Penela, MD, PhD

Role: CONTACT

Facility Contacts

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Antonio Berruezo, MD, PhD

Role: primary

93 290 62 51 ext. + 34

Other Identifiers

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SVC-RESCUE-AF

Identifier Type: OTHER

Identifier Source: secondary_id

SVC-RESCUE-AF

Identifier Type: -

Identifier Source: org_study_id

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