IVTCC 2.0: A Prospective Multicenter Ventricular Tachycardia Catheter Ablation Registry

NCT04520347 · tracked via the Priya Life Science Canada tracker

Sponsor

University of California, Los Angeles

Phase

Observational

Started

2018-12-01

Last updated

2025-12-15

Condition(s) studied

Ventricular ArrhythmiaVentricular TachycardiaPremature Ventricular Contraction (PVC)Cardiomyopathy

Study summary

This is a prospective multi-center international registry. The objective of this registry is to collect prospective data on patients undergoing catheter ablation for Ventricular Tachycardia (VT) and Premature Ventricular Contractions (PVC). The registry will be used for clinical monitoring, research, and quality improvement purposes.

Eligibility

Sex

ALL

Min age

—

Max age

—

Healthy volunteers

Inclusion Criteria: \- All patients undergoing catheter ablation for ventricular tachycardia (VT) or premature ventricular contractions (PVCs).

Primary outcome measure(s)

Ventricular tachycardia (VT) recurrence — From date of procedure assessed by shock, Anti-Tachycardia Pacing, or repeat procedure, up to 10 years.
Freedom from ventricular tachycardia episodes requiring ICD Intervention (shock or Anti-Tachycardia Pacing) or repeat procedure.

Trial sites (41)

Facility	City	Region
Banner Health, University of Arizona Medical Center	Phoenix	Arizona
Cedars-Sinai Medical Center	Los Angeles	California
University of California, Los Angeles	Los Angeles	California
University of California, Davis	Sacramento	California
University of California San Francisco	San Francisco	California
University of Colorado Hospital	Aurora	Colorado
Hartford HealthCare	Hartford	Connecticut
University of Florida Health	Gainesville	Florida
The Kansas City Heart Rhythm Institute	Kansas City	Kansas
University of Maryland Medical Center	Baltimore	Maryland
Johns Hopkins Heart and Vascular Institute	Baltimore	Maryland
Boston Children's Hospital	Boston	Massachusetts
Brigham and Women's Hospital	Boston	Massachusetts
Beth Israel Deaconess Medical Center	Boston	Massachusetts
UMass Memorial Health Care	Worcester	Massachusetts
University of Michigan Frankel Cardiovascular Center	Ann Arbor	Michigan
University of Minnesota VA Medical Center	Minneapolis	Minnesota
Mayo Clinic	Rochester	Minnesota
Washington University in St. Louis	St Louis	Missouri
The Mount Sinai Hospital	New York	New York
Columbia University Irving Medical Center	New York	New York
Montefiore Medical Center	The Bronx	New York
Cleveland Clinic Foundation	Cleveland	Ohio
Oregon Health & Science University	Portland	Oregon
Children's Hospital of Pennsylvania	Philadelphia	Pennsylvania
University of Pennsylvania Health System	Philadelphia	Pennsylvania
Wellspan Health	York	Pennsylvania
Medical University of South Carolina	Charleston	South Carolina
Vanderbilt Heart and Vascular Institute	Nashville	Tennessee
Texas Cardiac Arrhythmia Institute at St. David's Medical Center	Austin	Texas
Houston Methodist Hospital	Houston	Texas
University of Utah Health	Salt Lake City	Utah
University of Virginia Health System	Charlottesville	Virginia
University of Washington Medical Center	Seattle	Washington
The Montreal Heart Institute	Montreal	Canada
Shaare Zedek Medical Center	Jerusalem	Israel
Dokkyo Medical University Koshigaya Hospital	Koshigaya	Japan
Leiden University	Leiden	Netherlands
Erasmus Medical Center	Rotterdam	Netherlands
Gregorio Marañón General University Hospital	Madrid	Spain

+ 1 more sites — see the full list on the official registry below.

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04520347 on ClinicalTrials.gov ↗ ← All trials in Canada