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Does VoltagE Guided Additional Ablation Improve Procedural Outcome of Atrial Fibrillation Ablation?

Primary Purpose

Atrial Fibrillation

Status
Terminated
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Additional posterior wall isolation
Voltage-guided substrate homogenization
PVI only group
Sponsored by
Korea University Guro Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Catheter ablation, Atrial fibrillation, Low voltage area

Eligibility Criteria

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

Inclusion Criteria:

  • Patients undergoing first-time catheter ablation for AF.
  • Willing and able to provide informed consent
  • Age greater than or equal to 18 years.

Exclusion Criteria:

  • Patients who have previously undergone AF ablation
  • Patients with more than mild mitral valve stenosis or mechanical mitral valve replacement
  • Patients with chronic renal impairment with creatinine clearance rate of <30 mL/min
  • Patients who are pregnant

Sites / Locations

  • Korea University Guro Hospital
  • Korea University Anam Hospital
  • Bucheon Sejong Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Additional posterior wall isolation

Voltage-guided substrate homogenization

PVI only group

Arm Description

Operator will perform pulmonary vein isolation (PVI) and additional posterior wall isolation if low voltage area exists more than 10% of the left atrium

Operator will perform pulmonary vein antrum isolation (PVI) and additional substrate modification based on the degree of low voltage area.

Operator will perform PVI only

Outcomes

Primary Outcome Measures

Freedom rate of any atrial tachy-arrhythmia during 1 year after ablation procedure
Any recurrence of ECG or Holter documented atrial tachyarrhythmia* * Sustained AF or atrial tachycardia >30 s duration.

Secondary Outcome Measures

Procedure related complication rate
any adverse events
Total procedural time
total cumulative amount of radiation exposure

Full Information

First Posted
December 9, 2017
Last Updated
September 5, 2020
Sponsor
Korea University Guro Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03377751
Brief Title
Does VoltagE Guided Additional Ablation Improve Procedural Outcome of Atrial Fibrillation Ablation?
Official Title
Does VoltagE Guided Additional Ablation Improve Procedural Outcome of Atrial Fibrillation Ablation? (The VEGA-AF Study)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Terminated
Why Stopped
Majority of enrolled patients have withdrawn.
Study Start Date
February 15, 2018 (Actual)
Primary Completion Date
December 15, 2019 (Actual)
Study Completion Date
December 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Korea University Guro Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is designed to investigate whether pulmonary vein isolation(PVI) plus stepwise additional ablation approach based on the degree of low voltage area versus PVI only can improve procedure outcome in persistent atrial fibrillation(AF) patients.
Detailed Description
Catheter ablation of AF is well accepted and widely performing treatment method of AF at present. Pulmonary vein isolation (PVI) which aims to electrical isolation of pulmonary veins is currently the standard therapy for AF. But some researchers proposed additional ablation strategy for persistent AF (PeAF) because abnormal atrial substrate may play a role in these patients. However, there are inconsistent reports regarding a success rate of additional catheter ablation methods other than PVI. Thus, there still is no consensus on which strategy is appropriate in addition to PVI. One of these proposed options is complex fractioned atrial electrograms (CFAE) ablation. A meta-analysis of controlled trials comparing PVI alone versus PVI with CFAE reported that the addition of CFAE ablation results in a statistically significant increase in success rate for PeAF patients. Conversely, a prospective multicenter trial, The Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial Part II (STAR-AF II) trial showed that recurrence rate of AF following catheter ablation treatment was not significantly reduced when either linear ablation or ablation of CFAE was performed in addition to PVI. The investigators have previously reported that posterior wall isolation in addition to PVI plus linear lesions reduced recurrence of AF following catheter ablation compared to PVI only but the long-term success rate were markedly lower in the CFAE-guide ablation in addition PVI plus linear lesions group than in PVI plus linear lesions group among PeAF patients. Although benefit of addition CFAE could be originated from modification of abnormal atrial substrate which is generated by structural and electrical remodeling, this possible benefit could be counterbalanced by increased formation of transmural ablation scar which may result in dysfunction of left atrium and recurrence of atrial tachyarrhythmia. A recent study have showed that extent of myocardial injury by catheter ablation was associated with left atrium functional deterioration in patients with paroxysmal AF and myocardial damage provoked that may contribute to recurrence of AF following catheter ablation. Therefore, identification of PeAF patients who would benefit from additional ablation and tailored stepwise approach based on the identification may lead to reduction of iatrogenic myocardial injury and optimization of the result for the AF catheter ablation. Recent data have shown that voltage guided mapping of left atrium is a powerful predictor of AF recurrence after PAI and voltage based ablation strategy showed promising result in terms of tailored approach. But, prospective, randomized clinical studies are needed to compare the result of a voltage-based AF ablation to the result of established strategies.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
Catheter ablation, Atrial fibrillation, Low voltage area

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Additional posterior wall isolation
Arm Type
Experimental
Arm Description
Operator will perform pulmonary vein isolation (PVI) and additional posterior wall isolation if low voltage area exists more than 10% of the left atrium
Arm Title
Voltage-guided substrate homogenization
Arm Type
Experimental
Arm Description
Operator will perform pulmonary vein antrum isolation (PVI) and additional substrate modification based on the degree of low voltage area.
Arm Title
PVI only group
Arm Type
Active Comparator
Arm Description
Operator will perform PVI only
Intervention Type
Procedure
Intervention Name(s)
Additional posterior wall isolation
Intervention Description
PVI and additional posterior wall isolation will be performed according to the following protocol which is based on low voltage area. Proportion of low voltage area to area of left atrium body <10% : PVI only Proportion of low voltage area to area of left atrium body ≥10% : PVI + Posterior wall isolation Low voltage area will be measured from more than 1000 points of sampled voltage value during sinus rhythm using PentaRay catheter with 3D mapping system of CARTO (Biosense Webster, CA, USA).
Intervention Type
Procedure
Intervention Name(s)
Voltage-guided substrate homogenization
Intervention Description
PVI and additional substrate modification at low voltage areas will be performed according to the following protocol which is based on low voltage area. Proportion of low voltage area to area of left atrium body <10% : PVI only Proportion of low voltage area to area of left atrium body ≥10% : PVI + substrate homogenization at low voltage areas Low voltage area will be measured from more than 1000 points of sampled voltage value during sinus rhythm using PentaRay catheter with 3D mapping system of CARTO (Biosense Webster, CA, USA).
Intervention Type
Procedure
Intervention Name(s)
PVI only group
Intervention Description
PVI will be performed in this arm.
Primary Outcome Measure Information:
Title
Freedom rate of any atrial tachy-arrhythmia during 1 year after ablation procedure
Description
Any recurrence of ECG or Holter documented atrial tachyarrhythmia* * Sustained AF or atrial tachycardia >30 s duration.
Time Frame
Within 1 year after the ablation procedure
Secondary Outcome Measure Information:
Title
Procedure related complication rate
Description
any adverse events
Time Frame
during procedure and follow-up period(up to 1 year)
Title
Total procedural time
Description
total cumulative amount of radiation exposure
Time Frame
During procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing first-time catheter ablation for AF. Willing and able to provide informed consent Age greater than or equal to 18 years. Exclusion Criteria: Patients who have previously undergone AF ablation Patients with more than mild mitral valve stenosis or mechanical mitral valve replacement Patients with chronic renal impairment with creatinine clearance rate of <30 mL/min Patients who are pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hong Euy Lim, MD, Ph.D.
Organizational Affiliation
Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Korea University Guro Hospital
City
Seoul
State/Province
Guro-gu
ZIP/Postal Code
08308
Country
Korea, Republic of
Facility Name
Korea University Anam Hospital
City
Seoul
State/Province
Seongbuk-gu
ZIP/Postal Code
02841
Country
Korea, Republic of
Facility Name
Bucheon Sejong Hospital
City
Bucheon
ZIP/Postal Code
14754
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
No
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Does VoltagE Guided Additional Ablation Improve Procedural Outcome of Atrial Fibrillation Ablation?

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