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Impact of height and weight on acenocoumarol and phenprocoumon dose needed

Impact of height and weight on acenocoumarol and phenprocoumon dose needed - pre-EU-PACT study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32954
Enrollment
2000
Registered
2009-08-24
Start date
2009-11-10
Completion date
Unknown
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

atrial fribrillation Thrombosis

Interventions

None listed

Sponsors

Universiteit Utrecht
Lead Sponsor

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

MeasureTime frame
The impact of height and weight on the coumarin dose required. This will be investigated with lineair regression.

Secondary

MeasureTime frame
The dataset will be used as validation of the already developed acenocoumarol and phenrocoumon dosing algorithms.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)