Sickle Cell Disease Clinical Trial
Official title:
Assessment of Liver Fibrosis in Patients With Sickle Cell Disease
NCT number | NCT02007746 |
Other study ID # | 20120222 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | July 2012 |
Est. completion date | June 1, 2017 |
Verified date | May 2021 |
Source | University of Miami |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Patients with sickle cell disease many have a number of systemic complications, including liver problems. Some of these liver problems lead to liver fibrosis/cirrhosis, secondary to chronic blood transfusions. The purpose of this study is to investigate FibroScan readings in patients with sickle cell disease and iron overload secondary to blood transfusions, and to correlate the FibroScan results with Ferriscan. A comparison with the results of FibroScan to patients with Sickle cell without known liver disease, who have never been on chronic transfusions and with normal liver function profiles will also be made.The primary hypothesis is that the results of FibroScan will correlate with the results of Ferriscan and liver biopsy.
Status | Completed |
Enrollment | 26 |
Est. completion date | June 1, 2017 |
Est. primary completion date | June 1, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 10 Years to 65 Years |
Eligibility | Inclusion Criteria: - pediatric patients age 10 years and older with sickle cell disease - meeting other criteria: 1. history of chronic transfusion and iron overload and/or 2. known liver disease related to sickle cell or iron overload - signed consent and assent (as applicable) Exclusion Criteria: - children younger than 10 years - Pregnant females - Prisoners - Other causes of liver disease, unrelated to sickle cell or iron overload Inclusion criteria for controls: - Patients 10 years and older with sickle cell disease without history of chronic transfusions (less than 4 transfusions in a lifetime) - and without obvious liver disease. |
Country | Name | City | State |
---|---|---|---|
United States | University of Miami | Miami | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Miami |
United States,
Fraquelli M, Cassinerio E, Roghi A, Rigamonti C, Casazza G, Colombo M, Massironi S, Conte D, Cappellini MD. Transient elastography in the assessment of liver fibrosis in adult thalassemia patients. Am J Hematol. 2010 Aug;85(8):564-8. doi: 10.1002/ajh.2175 — View Citation
Voskaridou E, Plata E, Douskou M, Papadakis M, Delaki EE, Christoulas D, Terpos E. Treatment with deferasirox (Exjade) effectively decreases iron burden in patients with thalassaemia intermedia: results of a pilot study. Br J Haematol. 2010 Jan;148(2):332 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Liver transient elastography (FibroScan) of liver iron content and stiffness | Liver transient elastography (FibroScan) uses a probe consisting of an ultrasound transducer located at the end of a vibrating piston. The piston produces a vibration of low amplitude and frequency, which generate a shear wave that passes through the skin and liver tissue. The ultrasound then detects the propagation of the shear wave through the liver (at a depth of 25 - 65 mm below the skin surface) by measuring its velocity. The shear wave velocity is directly related to the tissue stiffness, with a higher velocity equating to higher tissue stiffness, corresponding to increasing severity of fibrosis. | at imaging visit (3 minutes) | |
Secondary | magnetic resonance imaging (MRI) measure of liver iron content and stiffness | at imaging visit (about 30-60 minutes) | ||
Secondary | liver function tests (ALT, AST, serum alkaline phosphate, GGTP, total bilirubin, direct bilirubin), complete blood count, platelets, reticulocyte count, serum ferritin to assess liver function and evaluate overall health | at clinic visit blood draw (about 1 minute) |
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