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ACTIVE NOT RECRUITING
NCT05038228

High Gastrointestinal Bleed Risk Outcomes in Patients With Non-valvular Atrial Fibrillation (NVAF) in France

Sponsor: Pfizer

View on ClinicalTrials.gov

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

Interventions

DRUG

Apixaban

Anticoagulant

DRUG

Rivaroxaban

Anticoagulant

DRUG

Dabigatran

Anticoagulant

DRUG

Vitamin K antagonist (VKA)

Anticoagulant

Locations (1)

Pfizer Investigator

London, United Kingdom