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Correction of thrombin generation in hemophilia plasma by recombinant factor V mutants

Correction of thrombin generation in hemophilia plasma by recombinant factor V mutants - Correction of thrombin generation in hemophilia plasma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30248
Enrollment
25
Registered
2006-10-12
Start date
2006-10-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

hemophilia

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Consenting adult patients with hemophilia A · 10 patients with severe hemophilia A (factor VIII 1.0 Bethesda Units)

Exclusion criteria

Exclusion criteria: Exclusion criteria · Liver disease leading to other coagulopathies · Anemia (Hb

Design outcomes

Primary

MeasureTime frame
Laboratory tests for activation of coagulation: - prothrombin activation fragment F1+2 (ELISA) - thrombin-antithrombin complexes (ELISA) - d-dimer (ELISA) - thrombin generation potential (amidolytic assay) - protein C dependent-thrombin generation potential (amidolytic assay) - routine coagulation tests (aPTT and PT) - factor V coagulant activity (one stage clotting test)

Secondary

MeasureTime frame
none

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)