NCT00512564|Completed
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Sponsor study identifier
observational
50
1 country
1
Study Start
September 2008
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
December 2010
Actual (reported)Study Completion
December 2010
Actual (reported)Iron overload is well study in Thalassemia patients and it's not only related to blood transfusions, since intestinal iron absorption is also increased in those patients. Sickle cell patients didn't developed significant clinical symptoms and signs of iron overload in spite frequent transfusions. The purpose of this study is to assess the iron overload in Sickle cell anemia and Sickle cell Thalassemia patients using clinical parameters and laboratory studies including Non Transferrin Binding Iron, Labile Iron and Hepcidin, in order to determine the cardiac and liver iron.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
December 2010
Actual (reported)Click on a node to explore related trials.
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
August 5, 2007
Actual (reported)August 7, 2007
Actual (reported)September 2008
Date type not reportedThis date has not been verified as actual or estimated.
December 2010
Actual (reported)December 2010
Actual (reported)Patients suffering from Sickle cell disease
Summary of clinical status related to iron overload and laboratory analysis of Iron overload including Total serum Iron, Transferrin, Ferritin and Non transferrin Binding Iron and Labile Plasma Iron
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
All tha patinets suffering from Sickle cell disease trreated at the Pediatric Hematology Unit
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Pediatric Hematology Unit - HaEmek Medical Center
Afula, Afula, 18101, Israel
Ariel Koren, MD
Pediatric Hematology Unit, Ha'Emek Medical Center
First Submitted
August 5, 2007
First Posted
August 7, 2007
Study Start
September 2008
Date type not reportedThis date has not been verified as actual or estimated.
Primary Completion
December 2010
Sickle Cell Anemia in an Arab Bedouin Village in the Northern Israel
Study Completion
December 2010
Actual (reported)Last Updated
August 26, 2011
Record last verified: 2011-08
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Source: ClinicalTrials.gov.
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