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Study identifier: NCT05799118 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Study of the Role of Genetic Modifiers in Hemoglobinopathies

Condition: Sickle Cell Disease · Thalassemia, Beta · Thalassemia Alpha  ·  Sponsor: Cyprus Institute of Neurology and Genetics

PhaseN/A
Planned participants30000
Who can joinAll sexes, 2 Years to no upper limit
Healthy volunteersNo

About this study

This study will investigate the role of genetic modifiers in hemoglobinopathies through a large-scale, multi-ethnic genome-wide association study (GWAS).

This description comes directly from the study's public registry record.

Talk to the study team

Petros Kountouris, PhD  ·  22392623  ·  admin@inherentnetwork.org

Always discuss trial participation with your own doctor first.

Locations (26)

Boston Children's HospitalBoston, Massachusetts, United StatesRecruiting
Lucrecia Paím MaternityLuanda, AngolaRecruiting
University of Buenos AiresBuenos Aires, ArgentinaNot Yet Recruiting
University Hospitals LeuvenLeuven, BelgiumNot Yet Recruiting
Universiti Brunei DarussalamBrunei, BruneiNot Yet Recruiting
Larnaca General HospitalLarnaca, CyprusRecruiting
Limassol General HospitalLimassol, CyprusRecruiting
Archbishop Makarios III HospitalNicosia, CyprusRecruiting
Paphos General HospitalPaphos, CyprusRecruiting
Centre Hospitalier MonkoleKinshasa, Democratic Republic of the CongoRecruiting
RigshospitaletCopenhagen, DenmarkRecruiting
Hippokrateio Hospital of AthensAthens, GreeceRecruiting

+ 14 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05799118