NCT02894450
Completed
Not Applicable
Study of Clinical and Laboratory Variables Associated With a Direct Oral Anticoagulant Bioassay (Xaban) Higher Among Those Aged Over 75 Years, as AOD for Atrial Fibrillation
ConditionsAtrial Fibrillation
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Atrial Fibrillation
- Sponsor
- Nantes University Hospital
- Enrollment
- 70
- Primary Endpoint
- bioassay direct oral anticoagulants
- Status
- Completed
- Last Updated
- 9 years ago
Overview
Brief Summary
The objective of this study was to investigate whether there is a link between clinical and biological variables and bioassay high xaban in elderly patients as part of an unscheduled hospitalization.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age ≥ 75 years
- •Entering SAU or MPG (Nantes University Hospital) as part of an unscheduled hospitalization for acute or subacute disease (About MPG, will be included patients admitted to the department within 48 hours of calling the doctor)
- •In xaban to entry (dabigatran, rivaroxaban, Apixaban) for non-valvular atrial fibrillation
- •In whom hemostasis tests will be prescribed as part of usual care
- •Patient has given its verbal agreement
- •Exclusion criteria
- •Patients with the following criteria may not be included:
- •Patients refusing to participate in the study
- •Patients under guardianship
- •Inability to obtain the date and time of the last dose of xaban
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
bioassay direct oral anticoagulants
Time Frame: Baseline
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