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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Sickle-cell Disease Registry of the GPOHCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, anemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, sickle cell diseaseRecruitingNot stated2025-01-24NCT03327428

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Research sitesCityCountryLinked trials
Center for Child and Adolescent Medicine, University Medical Center HeidelbergHeidelbergGermany1