Observational Study to Assess Sociodemographic and Clinical Features of Patients Treated With Rivaroxaban in Routine Clinical Practice of Hematologists, Cardiologists and Internists of Spain
NCT ID: NCT02262676
Last Updated: 2017-01-23
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
2251 participants
OBSERVATIONAL
2014-10-31
2015-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Rivaroxaban
Patients with Atrial fibrillation treated with Rivaroxaban
Rivaroxaban (Xarelto, BAY59-7939)
Patients treated by Physicians under approved local prescriptions
Interventions
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Rivaroxaban (Xarelto, BAY59-7939)
Patients treated by Physicians under approved local prescriptions
Eligibility Criteria
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Inclusion Criteria
* Patients with atrial fibrillation
* Patients in treatment with rivaroxaban for stroke prevention in atrial fibrillation at least 3 months previous to inclusion period in study
Exclusion Criteria
* Patients treated with other anticoagulant treatment
18 Years
ALL
No
Sponsors
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Janssen Research & Development, LLC
INDUSTRY
Bayer
INDUSTRY
Responsible Party
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Principal Investigators
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Bayer Study Director
Role: STUDY_DIRECTOR
Bayer
Locations
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Many Locations, , Spain
Countries
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Other Identifiers
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17671
Identifier Type: -
Identifier Source: org_study_id
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