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Thalassemia clinical trials

View clinical trials related to Thalassemia.

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NCT ID: NCT00971984 Completed - Hemolytic Anemia Clinical Trials

Demographic, Clinical and Laboratory Characteristics of Children With Alpha Thalassemia in Northern Israel

Start date: October 2009
Phase: N/A
Study type: Observational

The study intends to summarize the clinical and laboratory characteristics of children with hemolytic anemia diagnosed as having alpha thalassemia mutations.

NCT ID: NCT00971880 Completed - Sickle Cell Anemia Clinical Trials

Blood Transfusions in Thalassemia Patients, Complications and Adverse Effects

Start date: May 2009
Phase: N/A
Study type: Observational

Patients suffering from Thalassemia or another hemoglobinopathies required regular blood transfusions. The complications and adverse effects of blood transfusions can be classified as immediate and late. Among the immediate effects the most common are allergic reactions and fever, besides congestive heart failure in patients with cardiomyopathy. The late effects are mostly related to blood transmitted infections like HIV or Hepatitis C infections. The purpose of this study is to summarize the data of those complications in a cohort of 100 patients receiving regular blood transfusion.

NCT ID: NCT00971698 Completed - Sickle Cell Anemia Clinical Trials

The Spleen in Sickle Cell Anemia and Sickle Cell Thalassemia

Start date: February 2009
Phase: N/A
Study type: Observational

The spleen in Sickle Cell Anemia and Sickle Cell Thalassemia is usually enlarged in the first years of life but the immune protection provided is considered insufficient. In homozygous Sickle cell patients the spleen usually developed recurrent infarcts and after the first decade of age become fibrotic. Acute splenic sequestration is also frequent in those patients and this is considered as an indication for splenectomy. In comparison in Sickle cell thalassemia patients, hypersplenism is more frequent. The purpose of this study is to compare the clinical and laboratory issues related to the spleen in two groups of Sickle cell patients.

NCT ID: NCT00957931 Completed - Sickle Cell Disease Clinical Trials

Allo-HCT MUD for Non-malignant Red Blood Cell (RBC) Disorders: Sickle Cell, Thal, and DBA: Reduced Intensity Conditioning, Co-tx MSCs

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The main purpose of this project is to cure patients with high risk Sickle cell disease and other red cell disorders including thalassemia and diamond-blackfan anemia by bone marrow transplantation. The patients enrolled in this study will be those who lack matched sibling donors and therefore have no other option but to undergo bone marrow transplantation using matched but unrelated bone marrow or umbilical cord blood from the national marrow donor program registry. Since bone marrow transplantation for these disorders using matched unrelated donors has two major problems i.e. engraftment, or , the process of new marrow being accepted and allowed to grow in the the patient; and graft-versus-host disease, or the process where the new marrow "rejects" the host or the patient, this study has been devised with methods to overcome these two problems and thus make transplantation from unrelated donors both successful in terms of engraftment and safe in terms of side effects, both acute and long term. In order to accomplish these two goals, two important things will be done. Firstly, patients will get three medicines which are considered reduced intensity because they are not known to cause the serious organ damage seen with conventional chemotherapy. These medicines, however, do cause intense immune suppression so these can cause increased infections. Secondly, in addition to transplantation of bone marrow from unrelated donors, patients will also transplanted with mesenchymal stromal cells derived from the bone marrow of their parents. Mesenchymal stromal cells are adult stem cells that are normally found in the bone marrow and are thought to create the right background for the blood cells to grow. They have been shown in many animal and human studies to improve engraftment. In addition, they have a special property by which they prevent and are now even considered to treat graft versus host disease. Therefore, by using a reduced intensity chemotherapy regimen before transplant and transplanting mesenchymal stromal cells, we hope to improve engraftment while at the same time decrease the potential for severe side effects associated with a conventional transplant which uses extremely high doses of chemotherapy.

NCT ID: NCT00901199 Completed - Thalassemia Clinical Trials

Combined Chelation Therapy in Patients With Transfusion Dependent Thalassemia and Iron Overload

Start date: September 2007
Phase: Phase 2
Study type: Interventional

This is a pilot study looking at the safety and efficacy of giving combination chelation with deferasirox and deferoxamine. The hypothesis is that combination chelation is safe in decreasing overall iron in patients with thalassemia.

NCT ID: NCT00879242 Completed - Clinical trials for Beta Thalassemia Transfusion Dependent

Effect of Deferasirox on Patients With Cardiac MRI T2* < 20 Msec

Start date: February 2009
Phase: Phase 2
Study type: Interventional

This study will assess the safety and efficacy of deferasirox in patients with cardiac MRI T2* < 20 msec.

NCT ID: NCT00873041 Completed - Clinical trials for Non-transfusion Dependent Thalassemia

Efficacy and Safety of Deferasirox in Non-transfusion Dependent Thalassemia Patients With Iron Overload and a One Year Open-label Extension Study

THALASSA
Start date: November 2008
Phase: Phase 2
Study type: Interventional

CICL670A2209: This study will evaluate the safety and efficacy of deferasirox in non-transfusion dependent thalassemia patients with iron overload. Patients will be treated either with active treatment (deferasirox) or placebo for 12 months (core study phase). Patients who complete the core study phase will be offered to continue their study with the active treatment (deferasirox) in a 12 months extension phase. During the core and extension, the effects of treatment on iron overload in the liver will be evaluated using magnetic resonance imaging (MRI) assessments. CICL670A2209E1: A one-year open-label extension to a randomized, double-blind, placebo-controlled, phase II study to evaluate efficacy and safety of deferasirox in non-transfusion dependent thalassemia patients with iron overload (Thalassa).

NCT ID: NCT00872833 Completed - Thalassemia Clinical Trials

Assessment of Pain in People With Thalassemia Who Are Treated With Regular Blood Transfusions

Start date: July 2009
Phase: N/A
Study type: Observational

Thalassemia is an inherited blood disorder that can result in mild to severe anemia. Regular blood transfusions, which refresh the healthy red blood cell supply, are one treatment for thalassemia. People with thalassemia often experience pain, but the exact source of pain remains unknown. This study will examine how pain varies during the blood transfusion cycle in people with thalassemia who are treated with regular blood transfusions.

NCT ID: NCT00872339 Completed - Thalassemia Clinical Trials

Assessment of Pain in People With Thalassemia

Pain
Start date: March 2009
Phase: N/A
Study type: Observational

Thalassemia is an inherited blood disorder that can result in mild to severe anemia. People with thalassemia often experience pain, but the exact sources and prevalence of pain remain unknown. This study will examine the prevalence and severity of pain in people with thalassemia who are treated with regular blood transfusions and people with thalassemia who are not treated with regular blood transfusions.

NCT ID: NCT00872170 Completed - Clinical trials for Hypertension, Pulmonary

Sildenafil to Improve Exercise Capacity in People With Thalassemia and Pulmonary Hypertension

Start date: March 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Thalassemia is an inherited blood disorder that can result in mild to severe anemia. Many people with thalassemia also have pulmonary hypertension, which is high blood pressure in the arteries in the lungs. This study will evaluate the safety and effectiveness of the medication sildenafil at reducing blood pressure in the lungs of people with thalassemia and pulmonary hypertension.