NCT00481039|Completed
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Sponsor study identifier
observational
300
1 country
1
Study Start
May 2007
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
December 2008
Actual (reported)Study Completion
December 2008
Actual (reported)Sickle cell anemia and sickle cell thalassemia are frequent diseases among the israeli arab population. The purpose of this study is to assess the clinical characteristics of the patients in one arab village and the laboratory characteristics in the carriers of this gene based in the screening for pregnant women that is carried out in the population of northern Israel. The results can be useful in order to institute universal screening for sickle cell anemia in northern Israel.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
December 2008
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
May 2007
Date type not reportedThis date has not been verified as actual or estimated.
May 31, 2007
Actual (reported)June 1, 2007
Actual (reported)December 2008
Actual (reported)December 2008
Actual (reported)Patients diagnosed as having abnormal hemoglobin like hemoglobin S and thalassemia in a bedouin village
Medical history and basic laboratory analysis
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
All the patients diagnosed with abnormal hemoglobin in the bedouin arab village
Contact the study team to confirm eligibility.
Pediatric Hematology Unit - HaEmek Medical Center
Afula, 18101, Israel
Ariel Koren, MD
Pediatric Hematology Unit, Ha'Emek Medical Center
luci Zalman, Phd
Hematology Laboratory - HaEmek Medical Center
Tania Flaishman, Student
Pediatric Dpt B - Ha'Emek Medical Center
First Submitted
May 31, 2007
First Posted
June 1, 2007
Study Start
May 2007
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
December 2008
Actual (reported)Establishing a Repository of Blood and DNA Samples From People With Sickle Cell Disease (Comprehensive Sickle Cell Centers Collaborative Genotype-Phenotype Database and Sample Repository)
Study Completion
December 2008
Actual (reported)Last Updated
September 4, 2009
Record last verified: 2009-09
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Source: ClinicalTrials.gov.
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