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An analysis on distribution and inter-relationships of biomarkers under edoxaban in Japanese patients with non-valvular atrial fibrillatio

Not Applicable
Conditions
Patients with non-valvular atrial fibrillation who are taking edoxaban for prevention of ischemic stroke
Registration Number
JPRN-UMIN000028383
Lead Sponsor
Medical Science Department Daiichi-Sankyo Co. LTD.
Brief Summary

1) PC-Ed by LC-MS/MS was 194.3 (49.4-345.3) and 17.0 (4.8-40.7) ng/mL at peak and trough. 2) Correlation of PT with PC-Ed was higher than that of aPTT. 3) Among 6 PT reagents, Coagupia PT-N and Simplastin Excel S (both PT reagents) showed the highest predictive capability for the upper outlier of PC-Ed at peak and trough.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
106
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Receiving dual anti-platelet therapy (2) Inadequate dosage of edoxaban at registration (3) Edoxaban hypersensitivity (4) Patients who are bleeding (5) Patients with acute bacterial endocarditis (6) Renal dysfunction (creatinine clearance <30 mL/min) (7) River dysfunction with clotting disorder (8) Patients who had admitted with cardiovascular disease (stroke, myocardial infarction, PCI, and heart failure) or bleeding requiring hospitalization within 1 month before the registration (9) Patients who did not give written informed consents for this study (10) Patients who are judged by the researchers as inadequate for this study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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