DRKS00016741
Recruiting
Not Applicable
Exploratory study to assess frailty as a clinical marker for the plasma concentrations of the direct oral anticoagulants (Frailty-DOAK) - Frailty-DOAK
Agaplesion Bethanien Krankenhaus Geriatrisches Zentrum der Universität Heidelberg0 sites240 target enrollmentFebruary 20, 2019
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Frailty
- Sponsor
- Agaplesion Bethanien Krankenhaus Geriatrisches Zentrum der Universität Heidelberg
- Enrollment
- 240
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age \=70 years
- •Regular intake of one of the direct oral anticoagulants dabigatran (Pradaxa®), rivaroxaban (Xarelto®), apixaban (Eliquis®) or edoxaban (Lixiana®) during the past \= 7 days
- •Mentally and physically able to participate in the study (as judged by a member of the study group)
- •Written informed consent
Exclusion Criteria
- •Insufficient knowledge of written and/or spoken German
- •Inability to give informed consent
Outcomes
Primary Outcomes
Not specified
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