VIVO™ Accuracy Study
NCT03340142 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45
Last updated 2018-11-15
Summary
A multi-center study designed to assess the accuracy of VIVO™ in determining the location of a PVC/VT foci in comparison to an electroanatomical mapping system.
Conditions
- Premature Ventricular Contraction
- Ventricular Tachycardia
Interventions
- DEVICE
-
VIVO™
Diagnose the area of a PVC or VT onset
Sponsors & Collaborators
-
Catheter Precision. Inc.
lead INDUSTRY
Principal Investigators
-
Missiaen Huck · Catheter Precision. Inc.
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-01-29
- Primary Completion
- 2018-09-04
- Completion
- 2018-11-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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