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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Study of the Role of Genetic Modifiers in HemoglobinopathiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, alpha thalassemia spectrum, anemia, beta thalassemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, sickle cell disease, thalassemiaRecruitingNot stated2024-03-20NCT05799118

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Research sitesCityCountryLinked trials
Ahmadu Bello UniversityZariaNigeria1
Ampang HospitalAmpangMalaysia1
Archbishop Makarios III HospitalNicosiaCyprus1
Boston Children's HospitalBostonUnited States343
Centre Hospitalier MonkoleKinshasaDemocratic Republic of the Congo3
Centro Hospitalar e Universitário de CoimbraCoimbraPortugal2
Emek Medical CentreAfulaIsrael1
General Hospital Of LArissaLarissaGreece3
Hippokrateio Hospital of AthensAthensGreece1
Hospital Clínico San CarlosMadridSpain30
Kaduna State UniversityKadunaNigeria1
Laiko General HospitalAthensGreece2
Larnaca General HospitalLarnacaCyprus1
Limassol General HospitalLimassolCyprus1
Lucrecia Paím MaternityLuandaAngola1
National and Kapodistrian University of AthensAthensGreece10
Paphos General HospitalPaphosCyprus1
RigshospitaletCopenhagenDenmark84
Universiti Brunei DarussalamBruneiBrunei1
Universiti Kebangsaan MalaysiaBangiMalaysia1
Universiti Sains MalaysiaKota BharuMalaysia1
University Hospitals LeuvenLeuvenBelgium14
University of AbujaAbujaNigeria1
University of Buenos AiresBuenos AiresArgentina1
University of LahoreLahorePakistan1