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Ablation of Clinical Ventricular Tachycardia Versus Addition of Substrate Ablation on the Long Term Success Rate of VT Ablation (VISTA)

Primary Purpose

Ventricular Tachycardia

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Radiofrequency Catheter Ablation (RFCA)
Radiofrequency Catheter Ablation (RFCA)
Sponsored by
Texas Cardiac Arrhythmia Research Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ventricular Tachycardia

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Previous Myocardial infarction
  • Symptomatic, drug-refractory and haemodynamically stable VT following CAD
  • Undergoing a VT ablation
  • Implanted ICD

Exclusion Criteria:

  • Documented valvular heart disease
  • Acute myocardial infarction within the preceding 1 month
  • Unstable angina
  • Prolonged QT interval
  • Patients with hemorrhagic or thrombophilic disorders
  • Documented intra-atrial thrombus, tumor or other conditions which prevent easy catheter introduction

Sites / Locations

  • St.David's Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Clinical VT ablation

clinical VT and substrate ablation

Arm Description

Outcomes

Primary Outcome Measures

Recurrence of any sustained VT in the post-ablation period as demonstrated by electronic documentation Procedural complications associated with prolonged use of radiofrequency (RF) energy such as perforation, cardiac tamponade

Secondary Outcome Measures

Severe clinical events (hospital admissions for a cardiac cause, syncopal attacks, number of episodes of VT storms, death) Number of ICD interventions

Full Information

First Posted
January 8, 2010
Last Updated
August 21, 2014
Sponsor
Texas Cardiac Arrhythmia Research Foundation
Collaborators
University of Kansas, California Pacific Medical Center, Stanford University, Case Western Reserve University, Southlake Regional Health Centre, Catholic University, Italy, Ospedale dell'Angelo, Venezia-Mestre, RCCS Monzino Hospital, Milan, Italy, University of Rome Tor Vergata
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1. Study Identification

Unique Protocol Identification Number
NCT01045668
Brief Title
Ablation of Clinical Ventricular Tachycardia Versus Addition of Substrate Ablation on the Long Term Success Rate of VT Ablation
Acronym
VISTA
Official Title
Comparison of the Effect of Ablation of the Clinically Presenting Ventricular Tachycardia (VT) Only Versus the Addition of Substrate Ablation Based on Scar Mapping; on the Long Term Success Rate of VT Ablation
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas Cardiac Arrhythmia Research Foundation
Collaborators
University of Kansas, California Pacific Medical Center, Stanford University, Case Western Reserve University, Southlake Regional Health Centre, Catholic University, Italy, Ospedale dell'Angelo, Venezia-Mestre, RCCS Monzino Hospital, Milan, Italy, University of Rome Tor Vergata

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to assess whether a combined technique of substrate ablation and ablation of the clinically presenting VT at the site of early activation is superior to ablation of the clinically presenting VT alone, in enhancing long-term success of VT ablation.
Detailed Description
Background: VT is found mostly in patients with structural heart disease. It is classified using morphological criteria (monomorphic or polymorphic), duration of arrhythmia (sustained or non-sustained) or the mechanism of arrhythmia formation (re-entry, increased automation or triggered activity). The therapeutic approach and prognostic estimates of these different types of VT depend to a great degree on the mechanistic basis of the disease as well as the extent of myocardial damage and success of the therapy is measured by the absence of recurrence. Myocardial infarction with subsequent induction of VT is observed as a consequence of coronary artery disease (CAD). The infarct regions that are morphologically and electrically diseased can be arrhythmogenic and may form the substrate for macro-reentrant VT. Although antiarrhythmic drugs remain the primary form of therapy for VT, non-pharmacologic techniques like implantable cardioverter-defibrillator (ICD) and catheter ablation (CA) are becoming increasingly popular because of advancement in technology as well as an increase in desire among patients to eliminate the arrhythmia with ablation rather than suppressing it with drugs. ICDs and CA effectively terminate VT on a short-term basis; but multiple morphologies, hemodynamic instability and non-inducibility limit the long-term success rate of CA. The 'substrate mapping' approach defines areas of ventricular scar which can be potential VT sources. Several studies on small groups of patients have shown that successful ablation of VT substrates either reduces the recurrence of VT to 19- 50% or reduces the frequency of recurrence as well as the requirement of anti-arrhythmic drugs (AADs). Study design: This study is a multicenter, randomized, open label, parallel-arm clinical trial. A total of 120 post-myocardial infarction patients will be randomized at a 1:1 ratio into 2 groups: ablation targeting the clinically presenting VT at the site of early activation only, or ablation targeting the clinically presenting VT at the site of early activation plus substrate-based RF ablation Follow-up: Patients will undergo ICD interrogation at 3, 6 and 12 months to collect VT episode data, VT symptom assessment, complication assessment and AAD records. Management of AADs will be at the discretion of the physician.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ventricular Tachycardia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clinical VT ablation
Arm Type
Active Comparator
Arm Title
clinical VT and substrate ablation
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency Catheter Ablation (RFCA)
Intervention Description
RFCA of clinical VT
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency Catheter Ablation (RFCA)
Intervention Description
RFCA of clinical VT as well as VT substrates
Primary Outcome Measure Information:
Title
Recurrence of any sustained VT in the post-ablation period as demonstrated by electronic documentation Procedural complications associated with prolonged use of radiofrequency (RF) energy such as perforation, cardiac tamponade
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Severe clinical events (hospital admissions for a cardiac cause, syncopal attacks, number of episodes of VT storms, death) Number of ICD interventions
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Previous Myocardial infarction Symptomatic, drug-refractory and haemodynamically stable VT following CAD Undergoing a VT ablation Implanted ICD Exclusion Criteria: Documented valvular heart disease Acute myocardial infarction within the preceding 1 month Unstable angina Prolonged QT interval Patients with hemorrhagic or thrombophilic disorders Documented intra-atrial thrombus, tumor or other conditions which prevent easy catheter introduction
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Natale, MD FACC FHRS
Organizational Affiliation
TCAI, St.David's Medical Center, Austin, TX
Official's Role
Principal Investigator
Facility Information:
Facility Name
St.David's Medical Center
City
Austin
State/Province
Texas
ZIP/Postal Code
78705
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26718674
Citation
Di Biase L, Burkhardt JD, Lakkireddy D, Carbucicchio C, Mohanty S, Mohanty P, Trivedi C, Santangeli P, Bai R, Forleo G, Horton R, Bailey S, Sanchez J, Al-Ahmad A, Hranitzky P, Gallinghouse GJ, Pelargonio G, Hongo RH, Beheiry S, Hao SC, Reddy M, Rossillo A, Themistoclakis S, Dello Russo A, Casella M, Tondo C, Natale A. Ablation of Stable VTs Versus Substrate Ablation in Ischemic Cardiomyopathy: The VISTA Randomized Multicenter Trial. J Am Coll Cardiol. 2015 Dec 29;66(25):2872-2882. doi: 10.1016/j.jacc.2015.10.026.
Results Reference
derived

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Ablation of Clinical Ventricular Tachycardia Versus Addition of Substrate Ablation on the Long Term Success Rate of VT Ablation

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