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Clinical Trial Summary

Patients, who are adjusted to a new oral anticoagulant (Dabigatran, Rivaroxaban, Apixaban, Edoxaban) in routine treatment will recorded in this register. Within this register a characterization of patients (with regard to demography and indication) and therapy (with regard to medication, dose and duration) will be done. On basis of defined clinical relevant end points the long-term efficacy and safety will be evaluated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01588119
Study type Observational
Source GWT-TUD GmbH
Contact Jan Beyer-Westendorf, MD
Phone +49 351 458
Email jan.beyer@uniklinikum-dresden.de
Status Recruiting
Phase
Start date November 2011
Completion date December 2024