Ventricular Arrhythmia Ablation With the Use of Non-Invasive ECG Imaging Technology
Not Applicable
Withdrawn
- Conditions
- Ventricular TachycardiaPremature Ventricular Contraction
- Interventions
- Other: VIVO
- Registration Number
- NCT04219501
- Lead Sponsor
- Mayo Clinic
- Brief Summary
Researchers are trying to determine if the use of software called VIVO, made by Catheter Precision, Inc. can shorten the length of time it takes to perform an ablation procedure for either premature ventricular contractions (PVCs) and ventricular tachycardia (VT).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- At least 18 years of age
- Structurally normal heart
- Cardiac MRI/CT as part of standard of care
- Diagnosed with premature ventricular contractions or ventricular tachycardia and scheduled to undergo an ablation to treat these conditions
Exclusion Criteria
- Less than 18 years of age
- Structurally abnormal heart
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description VIVO Arm VIVO Subjects presenting for PVC/VT ablation, that have a previously acquired cardiac CT/MRI scan or are having a cardiac CT/MRI scan as per routine care, will undergo ablation procedures using VIVO, a novel, non-invasive mapping system.
- Primary Outcome Measures
Name Time Method VIVO non-invasive mapping system duration Baseline Total amount of time for non-invasive mapping using VIVO measured in minutes
Standard of care invasive electroanatomical mapping system duration Baseline Total amount of time for standard of care invasive mapping measured in minutes
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic in Florida
🇺🇸Jacksonville, Florida, United States