Sickle Cell Anemia in an Arab Bedouin Village in the Northern Israel

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-05-31

Study Completion Date

2008-12-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Sickle Cell Disease

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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1

Patients diagnosed as having abnormal hemoglobin like hemoglobin S and thalassemia in a bedouin village

Medical history and basic laboratory analysis

Intervention Type PROCEDURE

Medical history and basic laboratory analysis

Interventions

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Medical history and basic laboratory analysis

Intervention Type PROCEDURE

Eligibility Criteria

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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

Eligible Sex

ALL

Accepts Healthy Volunteers

No