Register for New Oral Anticoagulants (NOAC)

GWT-TUD

Status

Enrolling

Conditions

Anticoagulation Treatment

Study type

Observational

Funder types

Other

Identifiers

NCT01588119

NOAC

Details and patient eligibility

About

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.

Enrollment

5,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

indication for treatment with long term anticoagulation
initial adjustment or change to nex oral anticoagulant within routine treatment
indication for treatment with long term anticoagulation within the register:
permanent anticoagulation in arterial fibrillation
intended anticoagulation in acute venous thromboembolism for min. 3 months
other anticoagulation for min. 3 months within the approved indication

Exclusion criteria

missing Informed Consent Form
missing phone number for telephone follow up
contraindication for therapy with new oral anticoagulant (Dabigatran, Rivaroxaban, Apixaban, Edoxaban) according to Summary of Product Characteristics