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AF Substrate Mapping and Guided Ablation

Primary Purpose

Persistent Atrial Fibrillation

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Substrate+mCPVA
mCPVA
Sponsored by
Abbott Medical Devices
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Persistent Atrial Fibrillation focused on measuring atrial fibrillation, mapping, substrate, ablation

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 - 85 years of age
  • Persistent AF scheduled to undergo catheter ablation with approved standard indication by ESC/EHRA guidelines
  • First or second time ablation for persistent AF
  • Ability to provide written informed consent for study participation and be willing and able to comply with the study evaluations and follow up schedule

Exclusion Criteria:

  • Had two or more previous AF ablation procedures
  • Secondary AF
  • Hyperthyroidism
  • Left ventricular ejection fraction <30%
  • NYHA functional class IV
  • Left atrial area > 35 cm2
  • Uncorrected severe valvular heart disease
  • Contraindication to anticoagulation
  • Presence of left atrial thrombus
  • Recent (<6 Months) myocardial Infarction or unstable angina or coronary artery by-pass
  • Thoracic surgery for congenital, valvular or aortic disease
  • History of cerebrovascular accidents
  • Pregnancy
  • Significant comorbidities such as cancer, severe renal insufficiency requiring hemodialysis, severe obstructive lung disease, cirrhosis, with a life expectancy less than 2 years

Sites / Locations

  • I.R.C.C.S. Policlinico San Donato

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

mCPVA

Substrate+mCPVA

Arm Description

Subjects in the mCPVA arm will undergo intervention called "modified circumferential pulmonary vein ablation", which is considered to be the standard ablation treatment for AF.

Subjects in the Substrate+mCPVA arm will undergo intervention of substrate mapping and substrate-targeted ablation guided by the investigational device, followed by completion of modified circumferential pulmonary vein ablation.

Outcomes

Primary Outcome Measures

Long-term Clinical Success Rate
Freedom from symptomatic AF off antiarrhythmic drug therapy assessed from the end of the 3 months blanking period to 12 months following the ablation procedure, documented by implantable loop recorder (ILR) monitoring or trans-telephonic (TT) ECG monitoring.

Secondary Outcome Measures

Acute Ablation Procedure Outcome
Acute AF termination or significant AF cycle length slowing during RF application in ablation procedure

Full Information

First Posted
July 27, 2015
Last Updated
April 16, 2019
Sponsor
Abbott Medical Devices
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1. Study Identification

Unique Protocol Identification Number
NCT02571218
Brief Title
AF Substrate Mapping and Guided Ablation
Official Title
Substrate-Targeted Catheter Ablation to Treat Persistent Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
July 2015 (undefined)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
February 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Abbott Medical Devices

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In this study, the investigators aim to identify and characterize, by means of an EnSite Velocity Research Software, the electrophysiological characteristics of substrates that sustain AF in patients with persistent AF and to test whether ablation of such patient-specific substrates might improve the acute and long-term success of conventional catheter ablation therapy.
Detailed Description
This study is a prospective, single center, randomized, single-blind, controlled, 2-arm parallel group trial in Milan, Italy. The total duration of the study is expected to be 24 months with ~12 months of enrollment. Approximately 80 subjects suffering from persistent AF will be randomized in a 1:1 fashion to the following investigation arms: Modified circumferential pulmonary vein ablation alone (mCPVA); Substrate-targeted ablation guided by AF substrate mapping, followed by completion of modified circumferential pulmonary vein ablation (Substrate+ mCPVA) Ablate the areas that have fast and regular electrical activities, starting from the fastest cycle length (defined by Mean CL in the range of 120-250 milliseconds, and SD CL in the range of 1-30 milliseconds Ablate the areas that have consistent rotational or focal propagation pattern (defined by conduction velocity vectors) Ablate the areas that comprises the slow conduction zone of possible arrhythmia circuits If AF terminates during RF ablation, stimulation protocol will be used to examine if AF is re-inducible. If AF sustains or is re-inducible and physician decides to remap, mapping will be performed again for substrate-targeted ablation. If AF is not re-inducible, mCPVA will be completed Subjects will be followed up at 3, 6, 12 months. The primary objective of the study is to assess acute and long-term outcome of patient-tailored substrate-targeted ablation (Substrate) plus modified circumferential pulmonary vein ablation (Substrate+mCPVA) versus modified circumferential pulmonary vein ablation alone (mCPVA). The secondary objective of the study is to map and characterize electrophysiological substrates during AF, including regular and fast activities, complex fractionated electrograms, wave front propagation directions, and fibrosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persistent Atrial Fibrillation
Keywords
atrial fibrillation, mapping, substrate, ablation

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
mCPVA
Arm Type
Active Comparator
Arm Description
Subjects in the mCPVA arm will undergo intervention called "modified circumferential pulmonary vein ablation", which is considered to be the standard ablation treatment for AF.
Arm Title
Substrate+mCPVA
Arm Type
Experimental
Arm Description
Subjects in the Substrate+mCPVA arm will undergo intervention of substrate mapping and substrate-targeted ablation guided by the investigational device, followed by completion of modified circumferential pulmonary vein ablation.
Intervention Type
Device
Intervention Name(s)
Substrate+mCPVA
Intervention Description
The intervention in the experimental arm includes using a research software (investigational device) to map AF substrate and guide ablation.
Intervention Type
Device
Intervention Name(s)
mCPVA
Intervention Description
The intervention in the active comparator arm includes using the commercially available EnSite Velocity mapping and ablation system for modified circumferential pulmonary vein ablation.
Primary Outcome Measure Information:
Title
Long-term Clinical Success Rate
Description
Freedom from symptomatic AF off antiarrhythmic drug therapy assessed from the end of the 3 months blanking period to 12 months following the ablation procedure, documented by implantable loop recorder (ILR) monitoring or trans-telephonic (TT) ECG monitoring.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Acute Ablation Procedure Outcome
Description
Acute AF termination or significant AF cycle length slowing during RF application in ablation procedure
Time Frame
During Ablation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 - 85 years of age Persistent AF scheduled to undergo catheter ablation with approved standard indication by ESC/EHRA guidelines First or second time ablation for persistent AF Ability to provide written informed consent for study participation and be willing and able to comply with the study evaluations and follow up schedule Exclusion Criteria: Had two or more previous AF ablation procedures Secondary AF Hyperthyroidism Left ventricular ejection fraction <30% NYHA functional class IV Left atrial area > 35 cm2 Uncorrected severe valvular heart disease Contraindication to anticoagulation Presence of left atrial thrombus Recent (<6 Months) myocardial Infarction or unstable angina or coronary artery by-pass Thoracic surgery for congenital, valvular or aortic disease History of cerebrovascular accidents Pregnancy Significant comorbidities such as cancer, severe renal insufficiency requiring hemodialysis, severe obstructive lung disease, cirrhosis, with a life expectancy less than 2 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carlo Pappone, MD, PhD
Organizational Affiliation
I.R.C.C.S. Policlinico San Donato
Official's Role
Principal Investigator
Facility Information:
Facility Name
I.R.C.C.S. Policlinico San Donato
City
San Donato Milanese
State/Province
MI
ZIP/Postal Code
20097
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
29535136
Citation
Pappone C, Ciconte G, Vicedomini G, Mangual JO, Li W, Conti M, Giannelli L, Lipartiti F, McSpadden L, Ryu K, Guazzi M, Menicanti L, Santinelli V. Clinical Outcome of Electrophysiologically Guided Ablation for Nonparoxysmal Atrial Fibrillation Using a Novel Real-Time 3-Dimensional Mapping Technique: Results From a Prospective Randomized Trial. Circ Arrhythm Electrophysiol. 2018 Mar;11(3):e005904. doi: 10.1161/CIRCEP.117.005904.
Results Reference
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AF Substrate Mapping and Guided Ablation

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