GLORIA-AF Registry Program - Second and Third Phases
Status: | Active, not recruiting |
---|---|
Conditions: | Atrial Fibrillation, Neurology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/3/2019 |
Start Date: | November 7, 2011 |
End Date: | December 31, 2019 |
GLORIA - AF: Global Registry on Long-Term Oral Anti-thrombotic Treatment In Patients With Atrial Fibrillation (Phase II/III)
In this part of the Registry Program patients with non-valvular atrial fibrillation (AF) at
risk for stroke are enrolled to characterize the target population and to collect real world
data on important outcome events. For administrative purposes the study is divided into two
protocol numbers: 1160.129 for all non-EU (European Union) and non-EEA (European Economic
Area) countries, and 1160.136 for EU and EEA countries. The total number of patients enrolled
in both protocols is estimated to be 48,000 patients, and all these patients will be included
in the data analysis for study 1160.129.
risk for stroke are enrolled to characterize the target population and to collect real world
data on important outcome events. For administrative purposes the study is divided into two
protocol numbers: 1160.129 for all non-EU (European Union) and non-EEA (European Economic
Area) countries, and 1160.136 for EU and EEA countries. The total number of patients enrolled
in both protocols is estimated to be 48,000 patients, and all these patients will be included
in the data analysis for study 1160.129.
Inclusion criteria:
1. Age =>18 years at enrollment
2. Male or female patient (or legally acceptable representative) willing and able to
provide written informed consent
3. Patient newly diagnosed (< 3 months prior to baseline visit) with non-valvular AF and
at risk for stroke.
Other inclusion criteria apply.
Exclusion criteria:
1. Presence of any mechanical heart valve, or valve disease that is expected to require
valve replacement intervention;
2. Patients who have received more than 60 days of vitamin K antagonist (VKA) treatment
in their lifetime;
3. AF with a generally reversible cause;
4. Patients with a medical condition other than atrial fibrillation for which chronic use
of an oral anticoagulant (for example, a VKA) is indicated Other exclusion criteria
apply
We found this trial at
322
sites
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University of Chicago One of the world's premier academic and research institutions, the University of...
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University of Mississippi Medical Center The University of Mississippi Medical Center, located in Jackson, is...
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St Luke's - Roosevelt Hospital Center With 523 beds, Mount Sinai St. Luke's serves as...
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University of South Florida The University of South Florida is a high-impact, global research university...
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McFarland Clinic, PC It has been over 65 years since the founders of McFarland Clinic...
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2000 East Greenville Street
Anderson, South Carolina 29621
Anderson, South Carolina 29621
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21097 Northeast 27th Court
Aventura, Florida 33180
Aventura, Florida 33180
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Cooper University Hospital Cooper University Health Care, the clinical campus of Cooper Medical School of...
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University of Virginia Health System UVA Health System includes a 604-bed hospital, level I trauma...
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University of Illinois at Chicago A major research university in the heart of one of...
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University of Cincinnati The University of Cincinnati offers students a balance of educational excellence and...
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University of Texas Southwestern Medical Center UT Southwestern is an academic medical center, world-renowned for...
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Denver Health Medical Center Denver Health is a comprehensive, integrated organization providing level one care...
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446 North Reading Road
Ephrata, Pennsylvania 17522
Ephrata, Pennsylvania 17522
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5020 North Illinois Street
Fairview Heights, Illinois 62208
Fairview Heights, Illinois 62208
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1001 Sam Perry Boulevard
Fredericksburg, Virginia 22401
Fredericksburg, Virginia 22401
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