VIVO European Observational Registry

Catheter Precision

Status: Completed

Conditions: Ventricular Arrythmia; Premature Ventricular Contraction; Ventricular Tachycardia

Treatments: Device: VIVO

Study type: Observational

Funder types: Industry

Identifiers

NCT04990089

02-0521-001

Details and patient eligibility

About

A multi-center, observational registry conducted in Europe and the UK to prospectively review VIVO in a clinical setting in 125 patients.

Enrollment: 125 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients must at least 18 years of age Patients who have signed an IRB/EC approved patient informed consent and applicable patient privacy protection authorization per local law
• Patients who have previously had contrast cardiac imaging or will have cardiac imaging ordered per standard of care
• Patients will be selected without regard to gender.

Exclusion criteria

• Patients that are unable to receive contrast cardiac imaging (MR or CT)