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International study on etiology of inhibitors in patients with a moderate or mild form of hemophilia A, influences of immunogenetic and hemophilia treatment factors.

International study on etiology of inhibitors in patients with a moderate or mild form of hemophilia A, influences of immunogenetic and hemophilia treatment factors. - INSIGHT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32171
Enrollment
60
Registered
2008-06-23
Start date
2012-11-01
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

stollingsstoornissen bleeding disorder hemophilia A

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 99 Years

Inclusion criteria

Inclusion criteria: mild/moderate hemophilia A (factor VIII 2-40%)

Exclusion criteria

Exclusion criteria: severe hemophilia A (factor VIII

Design outcomes

Primary

MeasureTime frame
- The incidence of inhibitor development in mild/moderate hemofilia A. - Clinical and genetic risk factors that promote inhibitor development in mild/moderate hemofilia A. - T-cell epitopes in patients with mild/moderate hemophilia A and inhibitory antibodies.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)