RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) Episodes in the Cardiac Rhythm Management (CRM) Device Population

Abbott

Status: Completed

Conditions: Atrial Fibrillation

Treatments: Device: CRM Device

Study type: Observational

Funder types: Industry

Identifiers

NCT00837798

374

Details and patient eligibility

About

The purpose of this registry is to produce a prospective, outcome-oriented registry to document the prevalence of AT/AF in the CRM population by using the Advanced AT/AF Diagnostics in select SJM devices.

Enrollment: 5,379 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Patient is implanted with a CRM device
• Patient has no documented history of AF (3 months prior to enrollment)
• Patient is >18 years of age
• Patient has life expectancy of >24 months

Trial design

5,379 participants in 1 patient group

No history of AF

Description:

Patient should not have had a documented history of AF for a period of 3 months prior to enrollment.

Treatment:

Device: CRM Device