Alpha Thalassemia Clinical Trial
Official title:
Haplotype Analysis of Alpha Globin Genes in Israeli Ethnic Groups
Verified date | August 2017 |
Source | Hadassah Medical Organization |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Alpha thalassemia causes mild anemia and is found in many ethnic groups. Usually it is found
in regions where malaria is endemic. We have found that alpha thalassemia is common in
Ashkenazim, whose countries of origin are in temperate climates.
We are analyzing the alpha globin genes of individuals of many ethnic groups and will compare
to try to define the origin of thalassemia in these individuals of European extraction.
Status | Completed |
Enrollment | 100 |
Est. completion date | July 1, 2017 |
Est. primary completion date | July 1, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - diagnosis of deletional alpha thalassemia Exclusion Criteria: - under age 18 |
Country | Name | City | State |
---|---|---|---|
Israel | Hadassah Medical Organization | Jerusalem |
Lead Sponsor | Collaborator |
---|---|
Deborah Rund |
Israel,
Rund D, Filon D, Jackson N, Asher N, Oron-Karni V, Sacha T, Czekalska S, Oppenheim A. An unexpectedly high frequency of heterozygosity for alpha-thalassemia in Ashkenazi Jews. Blood Cells Mol Dis. 2004 Jul-Aug;33(1):1-3. — View Citation
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT02692872 -
Screening for Alpha Thalassemia in Healthy Volunteers
|