RATE Registry - Registry of Atrial Tachyarrhythmia/Atrial Fibrillation (AT/AF) Episodes in the Cardiac Rhythm Management (CRM) Device Population
NCT ID: NCT00837798
Last Updated: 2019-02-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
5379 participants
OBSERVATIONAL
2006-10-31
2012-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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No history of AF
Patient should not have had a documented history of AF for a period of 3 months prior to enrollment.
CRM Device
Pacemaker, ICD, or CRT device
Interventions
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CRM Device
Pacemaker, ICD, or CRT device
Eligibility Criteria
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Inclusion Criteria
* 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
18 Years
ALL
No
Sponsors
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Abbott Medical Devices
INDUSTRY
Responsible Party
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Principal Investigators
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Albert Waldo, MD
Role: STUDY_CHAIR
University Hospitals Cleveland Medical Center
Locations
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St Jude Medical
Sylmar, California, United States
Countries
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References
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Orlov MV, Olshansky B, Benditt DG, Kotler G, McIntyre T, Fujian Qu, Turkel M, Gorev M, Poghosyan H, Waldo AL. Is competitive atrial pacing a possible trigger for atrial fibrillation? Observations from the RATE registry. Heart Rhythm. 2021 Jan;18(1):3-9. doi: 10.1016/j.hrthm.2020.07.028. Epub 2020 Jul 30.
Swiryn S, Orlov MV, Benditt DG, DiMarco JP, Lloyd-Jones DM, Karst E, Qu F, Slawsky MT, Turkel M, Waldo AL; RATE Registry Investigators. Clinical Implications of Brief Device-Detected Atrial Tachyarrhythmias in a Cardiac Rhythm Management Device Population: Results from the Registry of Atrial Tachycardia and Atrial Fibrillation Episodes. Circulation. 2016 Oct 18;134(16):1130-1140. doi: 10.1161/CIRCULATIONAHA.115.020252.
Other Identifiers
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374
Identifier Type: -
Identifier Source: org_study_id
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