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Clot Formation and Clot Stability in Patients With Severe Haemophilia A

Clot Formation and Clot Stability in Patients With Severe Haemophilia A - Effect of Recombinant Factor VIII and Tranexamic Acid

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00279578
Enrollment
8
Registered
2006-01-19
Start date
2006-01-31
Completion date
2006-06-30
Last updated
2006-11-16

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

Conditions

Hemophilia A

Keywords

haemophilia A, thrombelastography, recombinant factor VIII, thrombin generation

Brief summary

In the present study we are examining the clot formation and clot stability in patients with severe haemophilia A after they receive recombinat factor VIII and after addition of tranexamic acid. Our hypothesis is that addition of tranexamic increases the clot stability. The perpective of the study is to document whether it is relevant to use traneksamic acid in surgery in patients with severe haemophilia A.

Detailed description

In the present study we are examining the clot formation and clot stability in patients with severe haemophilia A after they receive recombinat factor VIII and after addition of tranexamic acid. Our hypothesis is that addition of tranexamic increases the clot stability. The perpective of the study is to document whether it is relevant to use traneksamic acid in surgery in patients with severe haemophilia A.

Interventions

DRUGReFacto (Recombinant factor VIII) and Tranexamic acid

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Severe haemophilia A * Above 17 years old * Thrombocyt count above 100 x 109/l within the past two years

Exclusion criteria

* Received recombinant factor VIII with in the past 3 days * Inhibitor against recombinant factor VIII * HIV-positive * Ongoing treatment for hepatitis C * Known kidney disease * Allergy against Tranexamic acid * Not able to give informed consent

Design outcomes

Primary

MeasureTime frame
Clot stability

Secondary

MeasureTime frame
clot formation,thrombine generation

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026