atrial fibrillation
Conditions
Interventions
blood sampling once <
10 cc during the period of the clinical trial
Sponsors
Keio University School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with non-vitamin K antagonist oral anticoagulants
Exclusion criteria
Exclusion criteria: Equivalent to the drug indications
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The relationship among the coagulation tests, bleeding events, and thrombogenic events | — |
Countries
Japan
Contacts
Public ContactTakehiro Kimura
Keio University School of Medicine Department of Cardiology
Outcome results
None listed