EP Device Registry

Abbott

Status: Enrolling

Conditions: Cardiac Rhythm Disorder

Treatments: Other: Standard of Care

Study type: Observational

Funder types: Industry

Identifiers

NCT04460209

ABT-CIP-10316

Details and patient eligibility

About

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.

Enrollment: 7,500 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

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.