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Active, Not Recruiting

APIXABAN in the Prevention of Stroke and Systemic Embolism in Patients With Atrial Fibrillation in Real-Life Setting in France SNIIRAM Study - CV185-285

Updated: 27 November, 2018   |   ClinicalTrials.gov

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Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.

Trial Details

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
AC-experienced treated with apixaban
Drug: Apixaban
AC-experienced treated with dabigatran
Drug: dabigatran
AC-experienced treated with rivaroxaban
Drug: rivaroxaban
AC-experienced treated with VKA
Drug: VKA
AC-naive treated with apixaban
Drug: Apixaban
AC-naive treated with dabigatran
Drug: dabigatran
AC-naive treated with rivaroxaban
Drug: rivaroxaban
AC-naive treated with VKA
Drug: VKA

Key Eligibility Criteria

Inclusion Criteria: - Patient meeting inclusion criteria of the French Système national d'information inter-régimes de l'assurance maladie (SNIIR-AM)/Programme de médicalisation des systèmes d'information (PMSI) claim databases (Patient insured by the French national health insurance general scheme stricto sensu (apart from local mutualist sections) - Patients with at least one reimbursement of AC treatment (acenocoumarol, warfarine and fluidione for VKA treatments, apixaban, dabigatran or rivaroxaban for New oral anticoagulants (NOACs)) treatments during the inclusion period - Patients initiated with a new AC treatment during the inclusion period, either AC naive or not - Patients aged 18 or older at their first anticoagulant initiation during the inclusion period - Patient diagnosed with non-valvular Atrial fibrillation (AF)

We strongly recommend you contact BMS to report Side Effects (Adverse Events)
Side Effects (Adverse Events) and other reportable events are defined here
Report Side Effects (Adverse Events) or Product Quality Complaints: Medical Information

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