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Study was discontinued in 2018 as sufficient sample size was not met.
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Study of patients with nonvalvular atrial fibrillation (NVAF) who are newly prescribed NOACs (Novel Oral Anticoagulants) in routine clinical practice in England
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Participants with NVAF starting Apixaban |
| ||
| Participants with NVAF starting Warfarin |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Non-interventional | Other | Non-interventional |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of major bleeding | At the end of 1 year | |
| Incidence of intracranial bleeding | At the end of 1 year | |
| Incidence of gastrointestinal bleeding | At the end of 1 year | |
| Incidence of clinically relevant non-major bleeding | At the end of 1 year | |
| Incidence of ischemic stroke | At the end of 1 year | |
| Incidence of unspecified stroke | At the end of 1 year | |
| Incidence of systemic embolic events | At the end of 1 year |
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Inclusion Criteria:
Exclusion Criteria:
Other protocol defined inclusion/exclusion criteria could apply
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NVAF patients newly prescribed NOACs in England
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Local Institution | Bethesda | Maryland | 20814 | United States |
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| Label | URL |
|---|---|
| BMS Clinical Trial Information | View source |
| Investigator Inquiry Form | View source |
| FDA Safety Alerts and Recalls |
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| Non-Interventional |
| Other |
Non-Interventional |
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