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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00159029
Other study ID # 152910-HMO-CTIL
Secondary ID
Status Completed
Phase N/A
First received September 9, 2005
Last updated August 9, 2017
Start date April 1, 2004
Est. completion date July 1, 2017

Study information

Verified date August 2017
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Description:

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 polymorphisms to determine the haplotypes of individuals of many ethnic groups and will compare to try to define the origin of thalassemia in these individuals of European extraction.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Deborah Rund

Country where clinical trial is conducted

Israel, 

References & Publications (1)

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

See also
  Status Clinical Trial Phase
Active, not recruiting NCT02692872 - Screening for Alpha Thalassemia in Healthy Volunteers