Patients with atrial fibrillation after replacement with bioprosthetic valve.
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients who 3 months have passed after replacement with bioprosthetic valve (Aortic or Mitral valve replacement, surgical operation or TAVI) 2) Patients who have been given the definitive diagnosis of atrial fibrillation 3) Patients who can collect the data satisfied both 1) and 2) over 6 months.
Exclusion criteria
Exclusion criteria: 1) Patients who were participating in an interventional study during the period for investigation 2) Patients who have a mechanical valve in their body
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Development of stroke/systemic embolism and major bleeding during the observation period | — |
Countries
Japan
Contacts
DAIICHI SANKYO RD NOVARE CO., LTD. Clinical Development Department