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Sickle Cell Anemia clinical trials

View clinical trials related to Sickle Cell Anemia.

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NCT ID: NCT01783093 Completed - Clinical trials for Pulmonary Hypertension

Tricuspid Regurgitant Jet Velocity as an Independent Marker for Mortality in Sickle Cell Anemia

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

The purpose of this study is to evaluate patients with pulmonary hypertension and sickle cell disease who have had multiple echocardiograms. Previous studies have shown that an elevated tricuspid jet (TR) regurgitant velocity on echo in this population is a predictor of mortality. This initial data only examined an isolated TR jet velocity. It was presumed that the mortality was related to pulmonary hypertension. It is the aim of this study to retrospectively evaluate patients who have had multiple echocardiograms and to determine if patients who had either a normalization of their TR jet velocity on a subsequent echo or had no evidence of pulmonary hypertension on right heart catheterization had a similar mortality rate to those with persistently elevated TR jet velocity.

NCT ID: NCT01703104 Completed - Sickle Cell Anemia Clinical Trials

The Efficacy of Jobelyn (Sorghum Bicolor Extract)in the Treatment of Sickle Cell Anemia

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The primary objective is to determine if there is a significant increase in the haematocrit value of patients on Jobelyn and standard therapy compared to those on standard therapy alone.

NCT ID: NCT01547793 Completed - Sickle Cell Disease Clinical Trials

Carbon Monoxide Levels and Sickle Cell Disease Severity

Start date: January 26, 2012
Phase:
Study type: Observational

Background: - Some people with sickle cell disease have different health problems than others. This may be related to how easily and frequently the red blood cells break apart in the blood. Researchers want to test breath and blood samples from people with sickle cell disease to look for very small amounts of carbon monoxide, which is produced when red blood cells break apart. They will compare these results with breath samples from healthy volunteers. Studying different levels of carbon monoxide may help predict what health problems a person with sickle cell disease may get. It may also provide more information on possible treatments. Objectives: - To study breath carbon monoxide levels and their possible relation to the severity of sickle cell disease. Eligibility: - Individuals at least 18 years of age with sickle cell disease. - Healthy volunteers who are matched for age, sex, and race with the sickle cell disease group. Design: - Participants will be screened with a medical history. - Participants with sickle cell disease will provide a blood sample and have a heart function test. They will also breathe into a bag to provide an exhaled breath sample. - Healthy volunteers will provide an exhaled breath sample. - No treatment or care will be provided as part of this study.

NCT ID: NCT01527799 Completed - Sickle Cell Anemia Clinical Trials

Exercise Capacity in Pediatric Sickle Cell Anemia

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

The purpose of this study is to use comprehensive exercise testing to examine causes of exercise limitation in children and young adults with sickle cell anemia.

NCT ID: NCT01506544 Completed - Sickle Cell Anemia Clinical Trials

Pharmacokinetics (PK) of Liquid Hydroxyurea in Pediatric Patients With Sickle Cell Anemia

HU
Start date: December 2011
Phase: Phase 1
Study type: Interventional

Hydroxyurea (HU) is approved by the United States Food and Drug Administration (FDA) to treat adults with sickle cell anemia. Hydroxyurea has also been tested and used with children with sickle cell anemia. However, there are not many studies describing the disposition of drug in children less than 5 years old. The FDA has requested this study to better understand how children ages 2 to 17 years with sickle anemia absorb and eliminate the drug (this is called pharmacokinetics). The investigators will measure how much Hydroxyurea (HU) gets into the bloodstream at different time points after taking this medication.

NCT ID: NCT01479439 Completed - Sickle Cell Anemia Clinical Trials

Losartan to Reverse Sickle Nephropathy

Start date: February 2012
Phase: Phase 2
Study type: Interventional

Sickle cell disease causes kidney damage with increasing age, leading to chronic kidney disease and renal failure in nearly one third of patients with sickle cell disease. Currently, there is no treatment for sickle cell related kidney disease.

NCT ID: NCT01441375 Completed - Sickle Cell Anemia Clinical Trials

Sickle Cell Disease: A Retrospective Chart Review

Start date: July 2011
Phase: N/A
Study type: Observational

This study is a retrospective chart review of sickle cell patients and will include patients whom have received blood transfusions and those whom have not. Of the transfused patients, it will also include those whom have received chelation therapy and those whom have not.

NCT ID: NCT01356485 Completed - Sickle Cell Disease Clinical Trials

Safety Study of MP4CO in Adult Sickle Cell Patients

Start date: January 2012
Phase: Phase 1
Study type: Interventional

Sickle Cell Anemia is caused by an inherited hemoglobin disorder. Healthy red blood cells are discoid and can deform and move through small blood vessels to carry oxygen to all parts of the body. In sickle cell disease, as red blood cells circulate and oxygen is released in the circulatory system, the deoxygenated abnormal hemoglobin S can begin to polymerize. When this occurs, the red blood cells can become sticky and elongated. These sickled red blood cells are less flexible and will obstruct small blood vessels and block normal red blood cells from traveling through the circulatory system, which limits oxygen delivery to tissues and organs. This is known as a "sickle crisis". Patients suffering from a sickle crisis experience severe pain and are at risk of stroke, heart attack or even death. By lowering the level of oxygen pressure at which sickling occurs and opening the vasculature and rapidly delivering oxygen directly to ischemic tissues, the addition of MP4CO to existing treatment protocols may alleviate pain associated with a sickle cell crisis, abort a crisis and/or potentially reduce the duration of a crisis. This could mean less time in the hospital and an improved quality of life for patients with sickle cell anemia.

NCT ID: NCT01340404 Completed - Clinical trials for Cerebrovascular Accident

Allogeneic Genoidentical Stem Cell Transplantation in Children With Sickle-cell Anemia and Cerebral Vasculopathy

DREPAGREFFE
Start date: December 2010
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate that cerebral velocities assessed by transcranial doppler (TCD) are more significantly decreased by SCT than by long-term transfusion program A multicenter, national, non-randomized, prospective study of paired cohort will be conducted, with 2 groups of exposed (SCT) and non-exposed (TP) patients.

NCT ID: NCT01322269 Completed - Sickle Cell Disease Clinical Trials

A Study of HQK-1001 in Patients With Sickle Cell Disease

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of three dose levels of HQK-1001 administered once daily for 26 weeks in subjects with sickle cell disease.