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Thalassemia clinical trials

View clinical trials related to Thalassemia.

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NCT ID: NCT00512564 Completed - Sickle Cell Anemia Clinical Trials

Clinical and Laboratory Assessment of Iron Overload in Sickle Cell Anemia and Sickle Cell Thalassemia

Start date: September 2008
Phase: N/A
Study type: Observational

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.

NCT ID: NCT00512226 Completed - Sickle Cell Anemia Clinical Trials

Iron Overload Assesment in Sickle Cell Anemia and Sickle Cell Thalassemia

Start date: September 2007
Phase: N/A
Study type: Interventional

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 develope significant clinical symptoms and signs of iron overload in spite frequent transfusions. The purpouse of this study is to assess the iron overload in Sickle cell anemia and Sickle cell Thalassemia patients using clinical parameters and cardiac T2*MRI in order to determine the cardiac and liver iron.

NCT ID: NCT00502788 Completed - Hepatitis C Clinical Trials

Evaluating the Safety of Two Medications to Treat Hepatitis C in People With Thalassemia (The HepC Study)

HepC
Start date: May 2003
Phase: Phase 2
Study type: Interventional

Hepatitis C is one of the most common causes of long-term liver disease in the United States. Ribavirin and peginterferon alfa-2a are two medications that are used to treat hepatitis C infection. The purpose of this study is to evaluate the safety of these two medications in adults with hepatitis C and thalassemia, a type of blood disorder.

NCT ID: NCT00480974 Completed - Sickle Cell Anemia Clinical Trials

Long Term Follow up in Sickle Cell Patients Treated by Hydroxyurea

Start date: May 2007
Phase: N/A
Study type: Observational

Hydroxyurea was found to be a good treatment in adult patients with sickle cell anemia with significant decrease in the frequency of vaso-occlusive crises and other crises related to SCA. Several studies were published with relative short term follow up in pediatric and young adult age. The purpose of this study is to assess the long term follow up in a group of patients that initiated Hydroxyurea treatment in childhood.

NCT ID: NCT00480506 Completed - Thalassemia Major Clinical Trials

Monitoring of Erythroid Lineage Specific Chimerism Following Allogeneic Hematopoietic Transplantation for Thalassemia Major

Start date: April 2004
Phase: N/A
Study type: Observational

The purpose of this study is to collect peripheral blood and bone marrow aspirate samples from thalassemia patients in Tehran, in a collaborative effort to develop an erythroid lineage specific chimerism assay applicable to patients with thalassemia. Development of such an assay would be useful both for identification of the exact mutation causing the disease, as well as for providing a direct method to measure and monitor the kinetics of donor erythropoiesis in this patient population following transplant.

NCT ID: NCT00459732 Completed - Thalassemia Clinical Trials

Zinc & Bone Health in Thalassemia: The Think Zinc Study

ThinkZn
Start date: April 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether zinc can improve bone health in young patients with thalassemia.

NCT ID: NCT00456690 Completed - Thalassemia Clinical Trials

Endocrine and Nutritional Assessment in B Thalassemia Major

Start date: May 2007
Phase: N/A
Study type: Interventional

B Thalassemia patients developed short stature and low weight in spite no evident endocrine abnormalities. One hypothesis is that they developed some degree of malnutrition,then the purpose of this study is to assess the nutritional status before nutritional intervention and after one year. Siblings of the patients will serve as a control group. BMI, lipid and endocrine profile and leptin levels will be analysed in the study group only.

NCT ID: NCT00456443 Completed - Sickle Cell Anemia Clinical Trials

Invasive Infections in Children With Hemoglobinopathies

Start date: January 2006
Phase: N/A
Study type: Observational

Patients diagnosed as having hemoglobinopathies are exposed to serious bacterial infections, principally those patients that underwent splenectomy. Since the introduction of anti pneumococcal vaccine the incidence decreased significantly but other bacteria besides encapsulated bacteria takes place as principal cause of invasive infections. The purpose of this study is to analyse in a retrospective study the incidence of those infections in a group of patients suffering from thalassemia and sickle cell anemia treated in our clinic.

NCT ID: NCT00447694 Completed - Iron Overload Clinical Trials

Cardiac T2* in Beta-thalassemia Patients on Deferasirox Treatment

Start date: February 2006
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to evaluate changes in cardiac iron as measured by MRI T2* in beta-thalassemia patients with deferasirox treatment.

NCT ID: NCT00390858 Completed - Clinical trials for Transfusional Iron Overload

A 4-year Extension Study to Core 1-year Study of Iron Chelation Therapy With Deferasirox in β-thalassemia Major Pediatric Patients With Transfusional Iron Overload.

Start date: September 2003
Phase: Phase 2
Study type: Interventional

In this 4-year extension study the safety, efficacy and and pharmacokinetics of deferasirox in regularly transfused pediatric patients with β-thalassemia major was assessed. Patients who successfully completed the main 1 year trial (NCT00390858) were eligible to continue in this extension trial and receive chelation therapy with deferasirox for up to 4 years.