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Clinical Trials/NCT04686045
NCT04686045
Unknown
Not Applicable

Stroke Prevention in Atrial Fibrillation Patients Between 2004 and 2020

Jan Kochanowski University2 sites in 1 country10,000 target enrollmentJanuary 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation; Stroke Prevention
Sponsor
Jan Kochanowski University
Enrollment
10000
Locations
2
Primary Endpoint
oral anticoagulant treatment
Last Updated
5 years ago

Overview

Brief Summary

Prevention of thromboembolic complications is an important part in the management of patients with atrial fibrillation (AF). European and American guidelines recommend the use of non-vitamin K antagonist oral anticoagulants (NOACs) over therapy with vitamin K antagonists (VKA) in most AF patients. The number of patients treated with NOACs has increased significantly during the last few years. In the primary randomized controlled trials leading to their approval, compared to warfarin, NOACs were shown to be either noninferior or superior for stroke prevention in AF, with similar or reduced rates of bleeding, especially intracranial haemorrhage.

The aim of this study was to assess the frequency of oral anticoagulants using, espescially apixaban, dabigatran, and rivaroxaban, and the predictors of their prescription in a group of hospitalised patients with AF.

Registry
clinicaltrials.gov
Start Date
January 1, 2021
End Date
May 1, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Jan Kochanowski University
Responsible Party
Principal Investigator
Principal Investigator

Iwona Gorczyca

MD PhD

Jan Kochanowski University

Eligibility Criteria

Inclusion Criteria

  • non-valvular atrial fibrillation

Exclusion Criteria

  • valvular atrial fibrillation
  • death during hospitalization

Outcomes

Primary Outcomes

oral anticoagulant treatment

Time Frame: one year

Study Sites (2)

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