Multi-Center Study of Iron Overload: Survey Study (MCSIO)
NCT01913548 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 423
Last updated 2020-09-23
Summary
The purpose of this study is to demonstrate that a sufficient number of iron-overloaded thalassemia (THAL), Sickle Cell Disease (SCD)and Diamond Blackfan Anemia (DBA) populations with similar duration of chronic transfusion, and age at start of transfusions would be available for a confirmatory study. The study will examine the hypothesis that a chronic inflammatory state in SCD leads to hepcidin- and cytokine-mediated iron withholding within the RES (reticuloendothelial system), lower plasma NTBI (non-transferrin bound iron) levels, less distribution of iron to the heart in SCD.
Conditions
Sponsors & Collaborators
-
University College London (UCL) Cancer Institute
collaborator OTHER -
Universitätsklinikum Hamburg-Eppendorf
collaborator OTHER -
Medical University Innsbruck
collaborator OTHER -
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
collaborator NIH -
UCSF Benioff Children's Hospital Oakland
lead OTHER
Principal Investigators
-
Elliott Vichinsky, MD · UCSF Benioff Children's Hospital Oakland
-
John Porter, MD · University College London Cancer Institute
Eligibility
- Min Age
- 16 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-03-31
- Primary Completion
- 2013-08-31
- Completion
- 2013-10-31
Countries
- United States
- Germany
- United Kingdom
Study Locations
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