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Comparison of Operator-guided and Automatic Algorithm-guided Atrial Fibrillation Ablation

Primary Purpose

Atrial Fibrillation

Status
Completed
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Ablation using CARTO system
Sponsored by
Military Institute od Medicine National Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring atrial fibrillation, pulmonary vein isolation, RF ablation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with symptomatic atrial fibrillation qualified to catheter ablation according to current standards

Exclusion Criteria:

  • lack of informed consent
  • two previous pulmonary vein isolations

Sites / Locations

  • Military Institute of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Visitag group

Control group

Arm Description

Ablation using CARTO system. Visitag module: automated algorithm to collect RF ablation points using Visitag module. Criteria of ablation point: catheter stability range of motion ≤2.5mm, catheter stability time >15sec, contact force >5g over >50% of time. Optimal contact force suggested: 10-40g.

Ablation using CARTO system. Manual collection of RF ablation points by operator or by assistant. Optimal contact force suggested: 10-40g.

Outcomes

Primary Outcome Measures

AF recurrence
Number of AF recurrence after single catheter ablation during 12 months of follow-up.

Secondary Outcome Measures

Arrhythmia-free survival
Comparison of arrhythmia-free survival curves during the whole follow-up (even if extending over 1 year)

Full Information

First Posted
June 5, 2015
Last Updated
March 26, 2018
Sponsor
Military Institute od Medicine National Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02476227
Brief Title
Comparison of Operator-guided and Automatic Algorithm-guided Atrial Fibrillation Ablation
Official Title
Comparison of Operator-guided and Automatic Algorithm-guided Atrial Fibrillation Ablation. Randomized Open-labeled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
February 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Military Institute od Medicine National Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Catheter ablation in the treatment of atrial fibrillation (i.e. pulmonary vein isolation) is now the most effective method of prevention of arrhythmia recurrence. Use of 3D electroanatomical system is now a golden standard. Background hypothesis is that automatic algorithm collecting ablation points during pulmonary vein isolation (with certain catheter stability time, range of motion, and catheter-tissue contact force) prevents forming the gaps in the ablation line, thus preventing pulmonary vein reconnection and AF recurrence. The aim of the trial will be 1:1 comparison of the two methods of pulmonary vein isolation: with manual vs. automatic collection of ablation points using CARTO system and contact force catheter.
Detailed Description
Atrial fibrillation (AF) is the most common sustained supraventricular arrhythmia. It increases the risk of hospitalization and all-cause mortality. AF causes about 5-fold increase in the risk of stroke and 3-fold increase in the risk of heart failure. Catheter ablation in the treatment of AF (i.e. pulmonary vein isolation) is now the most effective method of prevention of arrhythmia recurrence, especially in paroxysmal AF. Still, efficacy of one procedure in a 1-year follow-up is between 20 and 80%, depending on demographic and clinical factors (concomitant diseases), and on the form of the arrhythmia (paroxysmal-persistent), it also depends on the method of ablation used and the experience of the centre. In a big European registry including over 1,300 patients antiarrhythmic drugs-free efficacy of catheter ablation in AF in 1-year follow-up was about 40%. Major finding in patients with AF recurrence after catheter ablation is pulmonary vein reconnection, so decreasing the risk of pulmonary vein reconnections seems crucial to diminish the risk of AF recurrence. Several novel technologies have been proposed lately to improve efficacy of AF ablation, their real importance needs validation in a clinical trial. Current standard is radiofrequency (RF) ablation with manual collection of ablation points (by operator or assistant). Automatic algorithm collect ablation points with additional criteria: catheter stability time, range of motion, and catheter-tissue contact force. The operator can see more precisely where the RF current has been applied and where are the gaps in the line. Background hypothesis is that automatic algorithm collecting ablation points (with certain catheter stability time, range of motion, and catheter-tissue contact force) prevents forming the gaps in the ablation line, thus preventing pulmonary vein reconnection and AF recurrence. The aim of the trial will be 1:1 comparison of the two methods of pulmonary vein isolation: with manual vs. automatic collection of ablation points using CARTO system and contact force catheter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
atrial fibrillation, pulmonary vein isolation, RF ablation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Visitag group
Arm Type
Experimental
Arm Description
Ablation using CARTO system. Visitag module: automated algorithm to collect RF ablation points using Visitag module. Criteria of ablation point: catheter stability range of motion ≤2.5mm, catheter stability time >15sec, contact force >5g over >50% of time. Optimal contact force suggested: 10-40g.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Ablation using CARTO system. Manual collection of RF ablation points by operator or by assistant. Optimal contact force suggested: 10-40g.
Intervention Type
Procedure
Intervention Name(s)
Ablation using CARTO system
Other Intervention Name(s)
RF ablation (CARTO system), Pulmonary vein isolation (CARTO system)
Intervention Description
automated algorithm (Visitag)-based vs. manual collection of RF ablation points during AF ablation
Primary Outcome Measure Information:
Title
AF recurrence
Description
Number of AF recurrence after single catheter ablation during 12 months of follow-up.
Time Frame
1-year follow-up after index procedure
Secondary Outcome Measure Information:
Title
Arrhythmia-free survival
Description
Comparison of arrhythmia-free survival curves during the whole follow-up (even if extending over 1 year)
Time Frame
Time to arrhythmia recurrence, follow-up 3-18 months after index procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with symptomatic atrial fibrillation qualified to catheter ablation according to current standards Exclusion Criteria: lack of informed consent two previous pulmonary vein isolations
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marek Kiliszek, MD, PhD
Organizational Affiliation
Military Institute of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Military Institute of Medicine
City
Warsaw
ZIP/Postal Code
04-141
Country
Poland

12. IPD Sharing Statement

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Comparison of Operator-guided and Automatic Algorithm-guided Atrial Fibrillation Ablation

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