Active, Not Recruiting
Study to Describe Risk of Bleeding in Patients Depending on the Different Anticoagulant Therapy They Are on for Atrial Fibrillation (AF) - CV185-664
Updated: 29 October, 2018 | ClinicalTrials.gov
Gender(s)
Age Range
Active, Not Recruiting
Inclusion Criteria: - Diagnosis of atrial fibrillation at or prior to index (the initiation of treatment) - Incident prescription of an oral anticoagulant (index date) - Patients with at least one year of computerized data prior to index date Exclusion Criteria: - Patients identified with a diagnosis of mechanical heart valve replacement or mitral stenosis identified at any point in the pre-index period in either CPRD by Read codes or in HES as ICD-10/OPCS codes - Patients with indication of venous thromboembolism (pulmonary embolism or deep vein thrombosis) identified in in either CPRD by Read codes or HES by ICD-10/OPCS codes within 3 months prior to index Other protocol defined inclusion/exclusion criteria could apply
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
