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

Registry of AT/AF Episodes in the CRM Device Population: RATE Registry

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00837798

Acronym

RATE

Enrollment

5379

Registered

2009-02-05

Start date

2006-10-31

Completion date

2012-04-30

Last updated

2019-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Brief summary

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.

Interventions

DEVICECRM Device

Pacemaker, ICD, or CRT device

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Prevalence of atrial tachycardia and atrial fibrillation in a cardiac rhythm management population	24 months

Secondary

Measure	Time frame
Development or exacerbation of HF	2 years
Development of AF	2 years
AT/AF burden	2 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026