GDF 15 in Sickle Cell Disease and Hereditary Spherocytosis
NCT ID: NCT01201135
Last Updated: 2010-09-14
Study Results
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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UNKNOWN
80 participants
OBSERVATIONAL
2010-09-30
2011-09-30
Brief Summary
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Detailed Description
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In iron-loading anemias, ineffective erythropoiesis suppresses hepcidin production, which result in dysregulating iron homeostasis. Miller and co-workers showed that release of cytokines like growth differentiation factor 15 (GDF15) during the process of ineffective erythropoiesis inhibits hepcidin production, thus defining a molecular link between ineffective erythropoiesis, suppression of hepcidin production and parenchymal iron loading.
Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Sickle cell disease
No interventions assigned to this group
hereditary spherocytosis.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
5 Years
ALL
No
Sponsors
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Wolfson Medical Center
OTHER_GOV
Responsible Party
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hematology department on Wolfsson Medical Center
Principal Investigators
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GHOTI HOSSAM, doctor
Role: PRINCIPAL_INVESTIGATOR
HEMATOLOGY DEPARTMENT ON WOLFSSON MEDICAL CENTER
Central Contacts
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Other Identifiers
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GDF-15CTIL
Identifier Type: -
Identifier Source: org_study_id