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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
The Severe Von Willebrand Disease (sVWD) Patient RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, blood coagulation disease, blood platelet disease, coagulation protein disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder, von Willebrand disease (hereditary or acquired), von Willebrand disease 3RecruitingNot stated2026-04-22NCT05437536

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OrganizationsLinked trials
VWD Connect Foundation1

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Research sitesCityCountryLinked trials
VWD Connect FoundationWellingtonUnited States1