why choose us

First received: May 12, 2023

Clinical Trial: Belgian Antithrombin Deficiency Registry

Study Status: NOT_YET_RECRUITING

Recruit Status: NOT_YET_RECRUITING

Condition: Antithrombin III Deficiency

Study Type: OBSERVATIONAL


Official Title: Antithrombin Registry - Investigation of Phenotype-genotype Correlations in Patients With Inherited Antithrombin Deficiency

Brief Summary: Inherited antithrombin deficiency is a rare autosomal dominant disorder that predisposes to the development of venous thromboembolism, even at young age.Inherited AT deficiency is considered the most severe form of inherited thrombophilia, increasing up to 40 times the risk of venous thrombosis.Our center has been performing research on antithrombin deficiency for several years.Therefore, it was decided to initiate a registry for patients with inherited antithrombin deficiency with the goal to gain more insight…

Read more