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Real world survey of Edoxaban for non-valvular atrial fibrillation patients using a Japanese healthcare database.

Not Applicable
Conditions
on-valvular atrial fibrillation
Registration Number
JPRN-UMIN000030744
Lead Sponsor
Daiichi Sankyo Co., Ltd Medical Science Department
Brief Summary

Total of 4,144 edoxaban-treated patients were matched with same number of warfarin patients and no-anticoagulant patients. Median follow-up period for the edoxaban arm, warfarin arm, and no-anticoagulant arm was 82, 39, and 324 days. For the comparison of the edoxaban and warfarin arms, and edoxaban and no-anticoagulant arm, no difference was found in the incidence of stroke/systemic embolism. The findings are limited by the short mean follow-up period in both treatment arms.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
4414
Inclusion Criteria

Not provided

Exclusion Criteria

1, Patients who underwent total knee replacement surgery 2, Patients who underwent total hip replacement surgery 3, Patients who underwent hip fracture surgery 4, Patients who have an artificial heart valves 5, Patients who have been given the diagnosis of rheumatic mitral valve diseases 6, Patients who have stroke, systemic embolism events, and/or bleeding events

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1,stroke 2,systemic embolism 3,bleeding
Secondary Outcome Measures
NameTimeMethod
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