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Stroke Prophylaxis of AF-patients: Real-life Effectiveness and Safety of Novel Anticoagulants Compared to VKA

Stroke Prophylaxis of Patients With Atrial Fibrillation: Real-life Effectiveness and Safety of Novel Anticoagulants Compared to Vitamin-k-antagonists Based on an Analysis of German Claims Data

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02657616
Enrollment
204464
Registered
2016-01-18
Start date
2015-12-31
Completion date
Unknown
Last updated
2016-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation, Stroke Prophylaxis

Brief summary

The central questions of the study can be summarized as follows: What stroke / death rates are the result of the use of the following treatment strategies: no anticoagulation with vitamin-k-antagonists (VKAs) or novel oral anticoagulants (NOACs), anticoagulation with VKAs and anticoagulation with NOACs (all). What other thromboembolic complication rates resulting from the use of these treatment strategies? What heavy bleeding rates resulting from the defined management strategies? The analysis is based on a data set of patients with atrial fibrillation (AF)(01/01/2010 - 30/06/2014). 2010 is used as the reference period and 01/01/2011-30/06/2013 as the inclusion period. The minimum observation time per patient is 12 months. Used is a data base of the AOK PLUS as well as the AOK Baden-Württemberg and AOK Bayern. The aim of the study is to compare clinical outcomes between the different treatment strategies (frequency of events and time to first event). The influence of alternative treatment strategies is measured on the basis of three different methodological approaches: unadjusted comparison of event council and time to first event between the defined patient groups; matched-pair comparison (propensity score matching) between the different groups of patients (treatment strategies) and multivariate analysis using time to event (Cox proportional hazards model) as the dependent variable.

Interventions

DRUGvitamin-k-antagonists
DRUGNovel oral anticoagulants

Sponsors

Institut für Pharmakoökonomie und Arzneimittellogistik e.V.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* one inpatient or two outpatient confirmed diagnosis of atrial fibrillation in two different quarters * Continuously insured by the AOK PLUS, AOK Bayern or AOK Baden-Württemberg

Exclusion criteria

* Age \< 18 years * Maximum possible observational period \< 12 months (exception: death)

Design outcomes

Primary

MeasureTime frame
Death01/01/2011-30/06/2014; at least 12 months; up to 40 months
Transient ischemic attack01/01/2011-30/06/2014; at least 12 months; up to 40 months
Ischemic stroke01/01/2011-30/06/2014; at least 12 months; up to 40 months
Hemorrhagic stroke01/01/2011-30/06/2014; at least 12 months; up to 40 months
Heavy bleeding01/01/2011-30/06/2014; at least 12 months; up to 40 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026