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ECG-I Targeted Ablation for Persistent AF (TARGET-AF)

Primary Purpose

Atrial Fibrillation

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
PVI followed by targeting of drivers
Sponsored by
Barts & The London NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Atrial Fibrillation ECG-I Mapping Catheter Ablation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Persistent AF (i.e. episodes of AF that are continuous for > 1 week)
  • Willing for ablation.
  • Age between 18 to 80.

Exclusion Criteria:

  • Duration of continuous persistent AF > 2 years
  • Left atrial diameter > 5 cm
  • Severe left ventricular impairment (EF < 40%)
  • New York Heart Association class 3 or 4 heart failure
  • Known hypertrophic cardiomyopathy, cardiac sarcoid or Arrhythmogenic cardiomyopathy.
  • Known inherited arrhythmia such as Brugada or long QT syndromes
  • Valvular disease that is more than moderate
  • History of valve replacement (metallic or tissue)
  • History of congenital heart disease (other than patent foramen ovale)
  • Previous left atrial ablation (percutaneous or surgical)
  • Cardiac surgery or percutaneous coronary intervention within the last 3 months.
  • Myocardial infarction or unstable angina within the last 3 months.
  • Unwillingness for ablation
  • Unwillingness to be involved in study
  • Suspected reversible cause of AF
  • Any other contraindication to catheter ablation
  • Age < 18 yrs or > 80 years
  • Pregnancy
  • Morbid obesity (defined as body mass index >40)
  • Any other medical problem likely to cause death within the next 18 months

Sites / Locations

  • Barts Heart Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

PVI followed by targeting of drivers

Arm Description

Patients will undergo intra-procedural mapping using the ECG-I. The pulmonary veins will be isolated. Drivers will then be targeted as guided by the ECG-I system aiming for termination of AF.

Outcomes

Primary Outcome Measures

Number of participants free from atrial arrhythmia (including AF and atrial tachycardia) at 12 months
Number of participants free from atrial arrhythmia (including AF and atrial tachycardia) at 12 months

Secondary Outcome Measures

Number of participants free from Atrial Fibrillation at 12 months
Number of participants free from Atrial Fibrillation at 12 months.
Termination of AF with PVI followed by ECGI guided driver ablation
Rates of termination of AF intra-procedurally during ablation
Composite end point including rates of AF termination and cycle length slowing with PVI followed by ECGI guided driver ablation
Rates of reaching composite end point (either termination of AF or cycle length slowing) intra-procedurally during ablation

Full Information

First Posted
November 11, 2020
Last Updated
November 11, 2020
Sponsor
Barts & The London NHS Trust
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1. Study Identification

Unique Protocol Identification Number
NCT04632680
Brief Title
ECG-I Targeted Ablation for Persistent AF
Acronym
TARGET-AF
Official Title
ECG-I Targeted Ablation for Persistent AF
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
March 31, 2021 (Anticipated)
Study Completion Date
June 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Barts & The London NHS Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Atrial fibrillation (AF) is an irregular heart rhythm associated with significant morbidity and mortality. Catheter ablation is an established treatment where catheters are inserted through a vein in the leg into the left atrium of the heart to deliver lines of scar to disrupt the tissue causing and maintaining AF. The ECG-I is a system which involves wearing a jacket with many ECG electrodes to record electrical activity from the surface of the body. A CT scan then shows where these electrodes are relative to the atria, and computer modelling is used to reconstruct the movements of electricity on the surface of the heart and therefore identifying where the drivers (tissue causing and maintaining AF) are located. Success rates for persistent atrial fibrillation lie in the region of 30-60% due to the location of drivers (tissue causing and maintaining AF) varying per patient. Locating and treating these drivers is very challenging. We intend to enrol 40 patients with persistent AF and perform atrial mapping using the ECG-I system. We will perform pulmonary vein isolation and perform atrial mapping to identify the location of these drivers and then to ablate them. We will study the effects of performing ablation upon these drivers using the ECG-I.
Detailed Description
Atrial Fibrillation (AF) is the commonest heart rhythm disturbance and is associated with significant morbidity and mortality. Catheter ablation (CA) is a procedure where catheters (leads) are passed into the heart and energy is used to disrupt and isolate (by freezing or cauterising) heart tissue causing AF. CA is an established therapy for AF. Success rates for CA for paroxysmal AF lies in the region of 70% or better. However, success rates for persistent AF is much lower and estimates lie in the region of 30-60%. Current CA protocols for AF centre on isolating the pulmonary veins (the pulmonary veins drain into the left atrium) which have been proven to trigger AF. Pulmonary Vein Isolation (PVI) ablation alone seems sufficient to remove the trigger for the vast majority of patients with paroxysmal AF. However, in patients with persistent AF it is common for AF to continue after the pulmonary veins have been electrically isolated. The difference in success rates between the paroxysmal and persistent form of AF is thought to be due to changes within the heart atria after AF has been established for some time. In persistent AF the atria dilate and remodel structurally and electrically, and therefore the maintenance of persistent AF differs from paroxysmal AF. Persistent AF is thought to be maintained by focal sources, whether rotors or sites of radial activation. Currently, targeting other sites within the atria in addition to PVI such as fractionated electrograms (areas of electrical activity) are thought to be imprecise and require extensive ablation. Often AF will persist despite targeting additional sites within the atria. Currently clinical characteristics of patients or structural imaging have limited accuracy in selecting patients likely to benefit from CA. Mapping studies have shown that patients with persistent AF who have higher frequency signals near the pulmonary veins than being distributed in the left atrial body are more likely to terminate to sinus rhythm (normal heart rhythm) with PVI alone and to maintain sinus rhythm. Studies have suggested that patients undergoing standard PVI ablation procedures for persistent AF who have coincidental interruption of drivers have a far better long term outcome. This suggests that the characteristics of atrial heart tissue and electrical activation patterns maintaining AF are likely to determine the response to ablation therefore it may be possible to determine more directly and accurately the likelihood of success by performing non-invasive mapping of the atria using the ECG-I. ECG-I is able to localise the drivers of AF and one of the objectives is to study the electrical characteristics of the tissue. ECG-I is currently being used in research into AF. A recently published a study using ECG-I to identify targets of ablation in 103 patients. They suggested that using ECG-I may improve CA success rates and reduces the procedure time and amount of ablation. The prospective multicentre AFACART study had similar findings. We intend to enrol 40 patients who will undergo Atrial Mapping with ECG-I during catheter ablation. After isolation of the pulmonary veins patients drivers will be targeted guided by the system.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
Atrial Fibrillation ECG-I Mapping Catheter Ablation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PVI followed by targeting of drivers
Arm Type
Experimental
Arm Description
Patients will undergo intra-procedural mapping using the ECG-I. The pulmonary veins will be isolated. Drivers will then be targeted as guided by the ECG-I system aiming for termination of AF.
Intervention Type
Device
Intervention Name(s)
PVI followed by targeting of drivers
Intervention Description
Patients will undergo intraprocedural ECG-I mapping. The pulmonary veins will be isolated followed by targeting of drivers aiming to terminate AF.
Primary Outcome Measure Information:
Title
Number of participants free from atrial arrhythmia (including AF and atrial tachycardia) at 12 months
Description
Number of participants free from atrial arrhythmia (including AF and atrial tachycardia) at 12 months
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of participants free from Atrial Fibrillation at 12 months
Description
Number of participants free from Atrial Fibrillation at 12 months.
Time Frame
12 months
Title
Termination of AF with PVI followed by ECGI guided driver ablation
Description
Rates of termination of AF intra-procedurally during ablation
Time Frame
During Catheter Ablation Procedure
Title
Composite end point including rates of AF termination and cycle length slowing with PVI followed by ECGI guided driver ablation
Description
Rates of reaching composite end point (either termination of AF or cycle length slowing) intra-procedurally during ablation
Time Frame
During Catheter Ablation Procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Persistent AF (i.e. episodes of AF that are continuous for > 1 week) Willing for ablation. Age between 18 to 80. Exclusion Criteria: Duration of continuous persistent AF > 2 years Left atrial diameter > 5 cm Severe left ventricular impairment (EF < 40%) New York Heart Association class 3 or 4 heart failure Known hypertrophic cardiomyopathy, cardiac sarcoid or Arrhythmogenic cardiomyopathy. Known inherited arrhythmia such as Brugada or long QT syndromes Valvular disease that is more than moderate History of valve replacement (metallic or tissue) History of congenital heart disease (other than patent foramen ovale) Previous left atrial ablation (percutaneous or surgical) Cardiac surgery or percutaneous coronary intervention within the last 3 months. Myocardial infarction or unstable angina within the last 3 months. Unwillingness for ablation Unwillingness to be involved in study Suspected reversible cause of AF Any other contraindication to catheter ablation Age < 18 yrs or > 80 years Pregnancy Morbid obesity (defined as body mass index >40) Any other medical problem likely to cause death within the next 18 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ross Hunter
Organizational Affiliation
Barts Heart Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Barts Heart Centre
City
London
ZIP/Postal Code
EC1A 7BE
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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ECG-I Targeted Ablation for Persistent AF

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