Atrial Fibrillation Clinical Trial
Official title:
Prospective Register Study to Record Safety and Efficacy of Oral Anticoagulants in Atrial Fibrillation Patients
NCT number | NCT03760874 |
Other study ID # | 19062013 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | June 13, 2013 |
Est. completion date | January 1, 2023 |
Verified date | June 2020 |
Source | University of Campania "Luigi Vanvitelli" |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
All patients with atrial fibrillation who are treated with vitamin-k antagonists (warfarin, phenprocoumon) or non vitamin K oral anticoagulants (Dabigatran, Rivaroxaban, Apixaban, Edoxaban) in real world settings will be recorded in this register. Within this register a characterization of patients 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.
Status | Recruiting |
Enrollment | 5000 |
Est. completion date | January 1, 2023 |
Est. primary completion date | January 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 110 Years |
Eligibility |
Inclusion Criteria: - Patients with atrial fibrillation - Indication for oral anticoagulant treatment Exclusion Criteria: - Missing Informed Consent Form - Missing Contact Informations for Follow up |
Country | Name | City | State |
---|---|---|---|
Italy | University of Campania "Luigi Vanvitelli" | Naples |
Lead Sponsor | Collaborator |
---|---|
University of Campania "Luigi Vanvitelli" | Monaldi Hospital |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Thromboembolic Events | 1 year | ||
Primary | Bleeding Events | 1 year |
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