EP Device Registry

Abbott Medical Devices5,003 enrolled

Overview

This study will provide ongoing, high quality data on the safety, performance, and clinical benefits of Abbott's EP devices in a real-world setting.

Study Type

OBSERVATIONAL

Enrollment

5,003

Conditions

Cardiac Rhythm Disorder

Interventions

Standard of CareOTHER

Standard of care mapping and/or ablation

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Subject underwent an electrophysiology imaging (diagnostic procedure) and/or ablation procedure that used one or more Abbott devices covered by this Registry. * Subject is willing and able to comply with the site's standard of care follow-up schedule. Exclusion Criteria: * Subject is currently participating in another clinical investigation that may confound the results of this Registry.

Locations (26)

KH Wiener Neustadt

Wiener Neustadt, Lower Austria, Austria

Outcomes

Primary Outcomes

The proportion of patients with a device- and/or procedure-related Serious Adverse Event

that occurred within 7-days of the procedure.

Time frame: 7-days

The proportion of procedures that achieved acute success.

Time frame: Baseline

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.