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Safety and Efficacy of Cryoballoon Pulmonary Vein Isolation : a Single Center Registry

Safety and Efficacy of Cryoballoon Pulmonary Vein Isolation : a Single Center Registry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03388658
Acronym
Gr-CryoFS
Enrollment
1003
Registered
2018-01-03
Start date
2007-11-30
Completion date
2017-05-31
Last updated
2018-01-03

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

Conditions

Atrial Fibrillation

Keywords

Atrial Fibrillation; Cryoballoon; Ablation;

Brief summary

The aim of this study was to assess the long-term success rates of pulmonary vein isolation using first and second generation cryoballoons in patients with paroxysmal and persistent atrial fibrillation.

Detailed description

The success of ablation is determined by the absence of recurrence of atrial fibrillation in the short term beyond 3 months, medium and long term on regular clinical follow-up and ECG holters. The patient cohort followed since 2007 allows a very long-term follow-up of patients who have benefited from atrial fibrillation cryoablation. Isolation of the pulmonary veins by cryoballoon (IVP) has emerged as an alternative to radiofrequency in the treatment of drug resistant atrial fibrillation (AF). (1) The potential benefits of cryoablation include shorter procedure times, decreased fluoroscopy time, shorter hospital duration, a different rate and type of complications compared to radio frequency offers potential benefits, including Including shorter procedure times, a decrease in the length of hospital stay 1 and a reduction in fluoroscopic time. (2) Effectiveness on a one year follow-up in cryoablation for AF is comparable to that of radiofrequency ablation in a prospective, randomized study with a lower major complication rate (3,4). The number of subjects is limited and most retrospective studies on cryoablation have a limited number of patients or an average follow-up not exceeding one year. Study of the data and results of the procedures of ablation of AF by cryoablation and long-term follow-up of the patients of the CHU of Grenoble. Regular monocentric cohort study based on collected data To identify the success rate of cryoablation ablation in paroxysmal and persistent AF

Interventions

None listed

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Patients with an indication for ablation of atrial fibrillation at the CHU of Grenoble since the use of this technique (November 2007) until November 2016: * Paroxysmal atrial fibrillation resistant to antiarrhythmic treatment. * Persistent atrial fibrillation. * Patients ≥18 years * Patients with discernment who signed consent for information on the ablation procedure before surgery.

Exclusion criteria

* patient less than 18 years old * patient who refused to sign informed consent for the procedure of ablation

Design outcomes

Primary

MeasureTime frameDescription
Long term efficacy of cryoballoon ablation for atrial fibrillation (AF)in a 8-year follow-up periodAbsence of recurrence (recurrence was defined as symptomatic or documented arrhythmia episode of\>30 seconds excluding a 3-month blanking period)

Secondary

MeasureTime frameDescription
Post procedure morbiditiesin a 8-year follow-up periodThe secondary outcomes include adverse events related to the procedure: death from any causes, atrial-oesophageal fistula, pericardial tamponade, neurological complication, phrenic nerve palsy, hematoma and vascular complications.
Cryoballoon 1 versus cryoballoon 2in a 1200-day follow-up periodComparison of acute and long term efficacy in of the first versus second generation cryoballoon -The success rate is evaluated at clinical follow-up and Holter, the efficacy of treatment is evaluated by per-ablation data. Total procedure times, catheter time in the left atrium, fluoroscopy time, cryoablation time are collected during the procedure and will be retrospectively analyzed with patient records and ablation records. The comparison will be made on the patient group having been treated with the new techniques and in particular the second generation balloon and those having been treated with the first generation balloon.
Clinical characteristics and predictive factors for success / complicationsin a 8-year follow-up periodThe clinical characteristics collected prospectively on the basis since 2007 will be analyzed retrospectively to evaluate one or more factors predicting success or complications of the procedure
Continuation of medical treatment post ablationin a 1200-day follow-up periodContinuation of anti-coagulant or anti-arrhythmic treatments beyond 3 months after the procedure will be collected

Countries

France

Outcome results

None listed

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