Viewing Study NCT00159029



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00159029
Status: COMPLETED
Last Update Posted: 2017-08-10
First Post: 2005-09-09

Brief Title: Genetics of Alpha Thalassemia in Israeli Ethnic Groups
Sponsor: Deborah Rund
Organization: Hadassah Medical Organization

Study Overview

Official Title: Haplotype Analysis of Alpha Globin Genes in Israeli Ethnic Groups
Status: COMPLETED
Status Verified Date: 2017-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None