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

Mayo Clinic

Status: Withdrawn

Conditions: Premature Ventricular Contraction; Ventricular Tachycardia

Treatments: Other: VIVO

Study type: Interventional

Funder types: Other

Identifiers

NCT04219501

19-007683

Details and patient eligibility

About

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).

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Control Group

No Intervention group

Description:

Subjects presenting for PVC/VT ablation will undergo ablation procedures using standard of care invasive electroanatomical mapping systems.

VIVO Arm

Experimental group

Description:

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.

Treatment:

Other: VIVO