Status:

COMPLETED

Hepcidin Levels in Sickle Cell Disease (SCD)

Lead Sponsor:

Kenneth Ataga, MD

Collaborating Sponsors:

Augusta University

Conditions:

Sickle Cell Anemia

Sickle - Beta Thalassemia

Eligibility:

All Genders

18-70 years

Brief Summary

The investigators propose that patients with HbSβ-thalassemia have lower levels of hepcidin and higher levels of GDF-15 than HbSS patients during the non-crisis, "steady states." In addition, the inve...

Detailed Description

Sickle cell disease (SCD) refers to a group of inherited disorders characterized by the presence of sickle hemoglobin (HbS) that are associated with episodes of acute illness and progressive organ dam...

Eligibility Criteria

Inclusion

  • age 18 - 70 years
  • confirmed diagnosis of HbSS or HbS-β thalassemia
  • no history of acute vaso-occlusive event (acute pain crisis or acute chest syndrome) requiring emergency room visit or hospitalization over the preceding 4 weeks
  • clinically acceptable physical examination and vital signs
  • ability of patient or legal representative to understand the requirements of the study and willingness to sign the Informed Consent document.

Exclusion

  • pregnancy or breastfeeding
  • current acute illness, including a painful crisis
  • iron deficiency anemia
  • history of liver disease with alanine aminotransferase (ALT) ≥ 3 X upper limit of normal (ULN)
  • history of hereditary hemochromatosis, connective tissues disease, chronic inflammatory, disorder, or malignancy
  • chronic transfusion program or any transfusion within the previous 3 months

Key Trial Info

Start Date :

March 1 2014

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 1 2015

Estimated Enrollment :

42 Patients enrolled

Trial Details

Trial ID

NCT02258997

Start Date

March 1 2014

End Date

September 1 2015

Last Update

October 8 2015

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Hepcidin Levels in Sickle Cell Disease (SCD) | DecenTrialz