Sickle Cell Anemia in an Arab Bedouin Village in the Northern Israel
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ClinicalTrials.gov Identifier: NCT00481039 |
Recruitment Status :
Completed
First Posted : June 1, 2007
Last Update Posted : September 4, 2009
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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.
Condition or disease | Intervention/treatment |
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Sickle Cell Disease | Procedure: Medical history and basic laboratory analysis |
Study Type : | Observational |
Estimated Enrollment : | 300 participants |
Observational Model: | Case-Only |
Time Perspective: | Retrospective |
Official Title: | Sickle Cell Anemia in an Arab Bedouin Village in the Northern Israel- An Observational Study |
Study Start Date : | May 2007 |
Actual Primary Completion Date : | December 2008 |
Actual Study Completion Date : | December 2008 |

Group/Cohort | Intervention/treatment |
---|---|
1
Patients diagnosed as having abnormal hemoglobin like hemoglobin S and thalassemia in a bedouin village
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Procedure: Medical history and basic laboratory analysis
Medical history and basic laboratory analysis |

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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- All the patients that were diagnosed as having sickle cell disease in the specific village and all the population screened for hemoglobinopathies in the same location

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00481039
Israel | |
Pediatric Hematology Unit - HaEmek Medical Center | |
Afula, Israel, 18101 |
Study Director: | Ariel Koren, MD | Pediatric Hematology Unit, Ha'Emek Medical Center | |
Study Chair: | luci Zalman, Phd | Hematology Laboratory - HaEmek Medical Center | |
Principal Investigator: | Tania Flaishman, Student | Pediatric Dpt B - Ha'Emek Medical Center |
Responsible Party: | Dr Koren Ariel, Pediatric Hematology Unit - Ha'Emek Medical Center |
ClinicalTrials.gov Identifier: | NCT00481039 |
Other Study ID Numbers: |
5311006.EMC |
First Posted: | June 1, 2007 Key Record Dates |
Last Update Posted: | September 4, 2009 |
Last Verified: | September 2009 |
Sickle cell disease Sickle cell thalassemia Population screening |
Anemia, Sickle Cell Anemia Hematologic Diseases Anemia, Hemolytic, Congenital |
Anemia, Hemolytic Hemoglobinopathies Genetic Diseases, Inborn |