I48.0 I48.1 I48.2 I48.3 I48.4 I48.9 I49.1 I49.2 I49.3 I49.4 I49.5 I49.8
Conditions
Interventions
Group 1: Diagnostic data, Treatment data, blood samples for biobanking, Questionnaires concerning Quality of life
Sponsors
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who undergo Treatment in the Atrial fibrillation unit > 18 years, existence of informed consent and signed consent document
Exclusion criteria
Exclusion criteria: Patients < 18 years, patients who can't understand the study documents, patients who don't sign the informed consent form
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Morbidity and Mortality (cause of death), follow up 12 months, any recurrence of arrhythmia, Major complications (Stroke, Bleeding, Myocardial infarction, pulmonary embolism) | — |
Secondary
| Measure | Time frame |
|---|---|
| Follow up of 30 days: cardiac complications (MACCE) Coronary artery disease, Stroke, TIA, pulmonary embolism), any recurrence of arrhythmia with Patient oriented combined endpoints, anticoagulation related complication (severe bleeding) | — |
Countries
Germany
Contacts
Public ContactKarsten Bock
Universitätsmedizin Mainz
Outcome results
None listed