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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
ATHNdataset RegistryCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Embolism and Thrombosis, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, X-linked disease, anemia, arthropathy, blood coagulation disease, blood platelet disease, cardiovascular disorder, coagulation protein disease, familial hemolytic anemia, hemarthrosis, hematologic disorder, hemolytic anemia, hemophilia A, hemophilia B, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder, inherited hemoglobinopathy, musculoskeletal system disorder, sickle cell disease, thrombotic disease, vascular disorder, vascular hemostatic disease, von Willebrand disease (hereditary or acquired)RecruitingNot stated2026-04-21NCT06820515