Clinical trials: Dysfibrinogenemia, Congenital
Hereditary Dysfibrinogenemia
Genomics of Fibrin Clot Structure in Patients With Constitutional Dysfibrinogenemia
Hereditary dysfibrinogenemia results from monoallelic mutation in one of the fibrinogen genes (FGA, FGB, FGG). The spectrum of molecular abnormalities is broad, leading to several subtypes of coagulation disorders with specific…
- Trial name
- GENDYSFIB (NCT05233384)
- Testing
- Blood test
- Where
- 7 sites in France
- Volunteers
- 70 people
- Sponsor
- University Hospital, Clermont-Ferrand
Hypofibrinogenemia, Congenital, Afibrinogenemia, Congenital
Pregnancy and Fibrinogen Disorders
The aim of this observational study is to evaluate the prevalence of uncomplicated pregnancies in women suffering from congenital fibrinogen disorders (i.e, hypofibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia) as well as…
- Conditions
- Hypofibrinogenemia, Congenital, Afibrinogenemia, Congenital, Dysfibrinogenemia, Congenital
- Trial name
- FIBRINOGEST (NCT03920332)
- Where
- 3 sites in France, Slovakia and 1 more
- Volunteers
- 149 people
- Sponsor
- University Hospital, Geneva