Z51.5
Conditions
Interventions
Group 1: Study participants are recruited during a consultation conducted by the Palliative Medicine Service (PMD) and the study team from the Department of Palliative Medicine at University Hospital
Sponsors
Palliativmedizin der Universitätsmedizin Essen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with metastatic solid tumor disease in specialized palliative care
Exclusion criteria
Exclusion criteria: - Concomitant therapy with vitamin K antagonists, heparins, argatroban, hirudin - Inability to provide consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of the proportion of patients with a NOAC medication whose plasma levels are within the target range. | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation between plasma levels of NOACs and clinical events such as strokes and TIAs. | — |
Countries
Germany
Contacts
Public ContactBaicy Mathew
Palliativmedizin der Universitätsmedizin Essen
Outcome results
None listed