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High Gastrointestinal Bleed Risk Outcomes in Patients With Non-valvular Atrial Fibrillation (NVAF) in France
Sponsor: Pfizer
Summary
This study is a retrospective analysis of observational cohorts using data from prospectively collected administrative/claims data to investigate treatment patterns, and safety and effectiveness outcomes in patients with NVAF with high risk of gastrointestinal bleed who initiate anticoagulant treatment with a Vitamin-K Antagonists (VKAs) or direct-acting oral anticoagulants (DOACs).
Official title: Anticoagulant Treatment Patterns and Outcomes Among Non-valvular Atrial Fibrillation Patients With High Risk of Gastrointestinal Bleeding in France: a Retrospective Cohort Analysis Using SNDS Database
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
1
Start Date
2022-08-01
Completion Date
2026-04-08
Last Updated
2026-03-12
Healthy Volunteers
No
Conditions
Interventions
Apixaban
Anticoagulant
Rivaroxaban
Anticoagulant
Dabigatran
Anticoagulant
Vitamin K antagonist (VKA)
Anticoagulant
Locations (1)
Pfizer Investigator
London, United Kingdom