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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04686045
Other study ID # The Jan Kochanowski Uniwersity
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date May 1, 2021

Study information

Verified date January 2021
Source Jan Kochanowski University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date May 1, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - non-valvular atrial fibrillation Exclusion Criteria: - valvular atrial fibrillation - death during hospitalization

Study Design


Related Conditions & MeSH terms


Intervention

Other:
observational study
observational study

Locations

Country Name City State
Poland 1st Clinic of Cardiology and Electotherapy Kielce Grunwaldzka 45
Poland Iwona Gorczyca Kielce

Sponsors (1)

Lead Sponsor Collaborator
Jan Kochanowski University

Country where clinical trial is conducted

Poland, 

Outcome

Type Measure Description Time frame Safety issue
Primary oral anticoagulant treatment one year