Atrial Fibrillation Clinical Trial
Official title:
Retrospective Registry Providing Baseline Data on the Outcome of Left Atrial (LA) or LA Appendage (LAA) Thrombus in Patients With Nonvalvular Atrial Fibrillation (AF) or Atrial Flutter After Standard of Care (SoC) Anticoagulant Therapy
Thrombus outcome data will be collected retrospectively during 2011-2012 as a historical
baseline of SoC with oral VKA (Vitamin K Antagonist(s) for the treatment of patients with
nonvalvular AF or atrial flutter documented with LA/ LAA thrombi on transesophag-eal
echocardiography (TEE).
The study is a company-sponsored, global, multi-center, retrospective, non-interventional
study. Patients who suffered from hemodynamically stable nonvalvular AF or atrial flutter
and had a diagnosed LA/ LAA thrombus between January 1st, 2011 and December 31st, 2012 will
be identified through screening and review of medical records and included in the registry.
Retrospective patient data will be collected from May 2nd, 2013 to May 2nd, 2014. The
observation of each patient will cover the period from the diagnosis of an LA/ LAA thrombus
until the end-of-treatment TEE following the 3-12 week SoC anticoagulation (AC) therapy. If
no end-of-treatment TEE has been performed during 3-12 weeks of AC therapy, the
observational period will end at 12 weeks after diagnosis at the latest. If more than one
TEE was performed during treatment, the thrombus outcome will be collected from the last TEE
performed within 12 weeks of treatment start.
n/a
Time Perspective: Retrospective
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