atrial fribrillation Thrombosis
Conditions
Interventions
None listed
Sponsors
Universiteit Utrecht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: INR target between 2.5 and 3.5 18 years or older no participation at vitamin K study (VIKS2A)
Exclusion criteria
Exclusion criteria: Pregnancy or lactation Severe cognitive impairment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The impact of height and weight on the coumarin dose required. This will be investigated with lineair regression. | — |
Secondary
| Measure | Time frame |
|---|---|
| The dataset will be used as validation of the already developed acenocoumarol and phenrocoumon dosing algorithms. | — |
Countries
Netherlands
Outcome results
None listed