VIVO European Observational Registry

NCT ID: NCT04990089

Last Updated: 2025-01-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

125 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-10-21

Study Completion Date

2024-09-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Ventricular Arrythmia Ventricular Tachycardia Premature Ventricular Contraction

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

VIVO

VIVO is a per-procedural planning tool designed to non-invasively identify the origin of a ventricular arrhythmia.

Intervention Type DEVICE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Catheter Precision. Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Andre Ng, MD

Role: PRINCIPAL_INVESTIGATOR

Glenfield University Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Mater Private Hospital

Dublin, , Ireland

Site Status

Mazzoni Hospital

Ascoli Piceno, , Italy

Site Status

University Medical Center Groningen

Groningen, , Netherlands

Site Status

Erasmus Medical Center

Rotterdam, , Netherlands

Site Status

La Luz Hospital

Lisbon, , Portugal

Site Status

Glenfield University Hospital

Leicester, , United Kingdom

Site Status

Royal Brompton Hospital

London, , United Kingdom

Site Status

John Radcliffe University Hospital

Oxford, , United Kingdom

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Ireland Italy Netherlands Portugal United Kingdom

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

02-0521-001

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

END - VT Cohort Study
NCT05835791 RECRUITING