Study of the Role of Genetic Modifiers in Hemoglobinopathies

Recruiting Observational Study
Sickle Cell Disease Thalassemia, Beta Thalassemia Alpha Hemoglobinopathies
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
2 and older
Sex
Any
Study type
Observational
Participants needed
30,000 (estimated)
Sponsor
Cyprus Institute of Neurology and Genetics · Other
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About This Trial

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

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Clinical diagnosis of an inherited hemoglobinopathy, including sickle cell disease (SCD), β-thalassemia, and α-thalassemia; all genotypes will be considered. * Age ≥ 2 years old at the time of the collection of the phenotypic data. * There will be no limits on study participan…
Contacts

Petros Kountouris, PhD

22392623

admin@inherentnetwork.org

CONTACT