Ventricular Arrhythmia Ablation With the Use of Non-Invasive ECG Imaging Technology

Not Applicable

Withdrawn

• Conditions: Ventricular Tachycardia; Premature Ventricular Contraction

• 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

Study Timeline

• Study First Submitted: 2020-01-03
• Study First Submitted QC: 2020-01-03
• Study First Posted: 2020-01-07
• Study Start: 2021-02-01
• Status Verified: 2021-03
• Last Update Submitted: 2021-03-04
• Last Update Posted: 2021-03-08
• Primary Completion: 2022-12-31
• Study Completion: 2022-12-31

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• Status: WITHDRAWN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

Primary Outcome Measures

Name	Time	Method
Standard of care invasive electroanatomical mapping system duration	Baseline	Total amount of time for standard of care invasive mapping measured in minutes
VIVO non-invasive mapping system duration	Baseline	Total amount of time for non-invasive mapping using VIVO measured in minutes

Trial Locations

Locations (1)

Mayo Clinic in Florida; 🇺🇸 Jacksonville, Florida, United States