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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Evaluation of an Information Management and Communication System for Population-wide Point-of-Care Infant Sickle Cell Disease ScreeningCongenital, 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 applicable2026-05-27NCT07610239