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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Belgian Antithrombin Deficiency RegistryBlood Protein Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, blood coagulation disease, hematologic disorder, hereditary antithrombin deficiency, hereditary disease, inherited blood coagulation disorder, thrombophiliaNot yet recruitingNot stated2024-12-04NCT05891899

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OrganizationsLinked trials
Universitair Ziekenhuis Brussel114

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Research sitesCityCountryLinked trials
UZ BrusselBrusselsBelgium45