A Phase 2 interventional study of RBC transfusion in Pulmonary Hypertension and Sickle Cell Disease, sponsored by University of North Carolina, Chapel Hill. Withdrawn. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2013-07-29.
Sponsored by University of North Carolina, Chapel Hill · Phase 2, Interventional, and Treatment
Pulmonary hypertension, a complication associated with an increased risk of death, is common in patients with sickle cell disease. Despite its frequency, there remains no standard treatment for this complication in patients with sickle cell disease.
In this small study, the investigators will evaluate the effect of monthly transfusion of red blood cells to patients with sickle cell disease-associated pulmonary hypertension. The investigators speculate that by increasing the hemoglobin level and decreasing the amount of sickle red blood cells, these patients would experience improvements in their PHT.
As patients with sickle cell disease (SCD) age, recurrent vaso-occlusive episodes lead to progressive end-organ damage. Pulmonary hypertension (PHT) represents an example of such end-organ damage. Pulmonary hypertension, a common complication in patients with sickle cell disease (SCD), results in a shortened survival. The high mortality reported in SCD patients with PHT appears to occur particularly in those patients with moderate and severe elevations in their pulmonary artery pressure. The overall objective of this proposal is to evaluate the effect of chronic red blood cell transfusion on PHT in SCD. We hypothesize that by increasing the hemoglobin concentration and decreasing the amount of HbS, these patients would experience improvements in their PHT.
Thus, the specific aim of this clinical trial is to evaluate the effects of RBC transfusion on pulmonary hypertension in SCD, as well as the effect of chronic RBC transfusion on plasma markers of thrombin generation, platelet activation, and nitric oxide metabolites.
Study subjects will be transfused monthly for 6 months to investigate the safety and efficacy of RBC transfusion in SCD patients with PHT. All packed red blood cells will have extended antigen matching for C, D, E and Kell to minimize the risk of alloimmunization. Subjects will receive other routine treatments for SCD. Specific outcome variables will be evaluated at 1 month, 3 months, and 6 months. All study subjects will receive simple transfusion of packed red blood cell to achieve a post-transfusion hemoglobin (Hb) not greater than 10 g/dL. For those subjects who may have baseline hemoglobins in whom a post transfusion Hb would exceed 10 g/dL, they will require a limited exchange transfusion, i.e. phlebotomy of 1 unit of blood, followed by transfusion of 2 units of packed RBC. All study subjects will return for assessment of safety and/or efficacy measures every two weeks for the first month, and subsequently every four weeks till the completion of the study. Study subjects who experience a documented worsening of their disease (decreased SaO2, worsening 6-minute walk) on at least two consecutive follow up visits will be taken off the study. At the end of the study, subjects will have the option of continuing on chronic RBC transfusion.
1,105 studies on the registry are indexed under Hypertension, Pulmonary; 234 are open to participants now.
Browse Hypertension, Pulmonary studies →University of North Carolina, Chapel Hill is the lead sponsor of 1,340 studies on the registry; 133 are open to participants now.
Of its 155 completed or terminated interventional studies of FDA-regulated products, 136 (88%) have results posted.
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Exclusion Criteria:
All subjects wil receive monthly RBC transfusions for 6 months
Other: RBC transfusion
Study subjects will receive monthly transfusions with 2 units of red blood cells
Pulmonary artery systolic pressure (mm Hg)
Time frame: 2 years
Pulmonary vascular resistance (dyne.s.cm-5)
Time frame: 2 years
Six-minute walk
Time frame: 2 years
Markers of thrombin generation (TAT complexes, F1.2, d-dimers)
Time frame: 2 years
Markers of platelet activation (soluble CD40 ligand, beta thromboglobulin, platelet factor
Time frame: 2 years
Nitric oxide metabolites
Time frame: 2 years
Quality of life
Time frame: 2 years
No study locations are listed for this record.
This study is withdrawn, as verified in Jul 2013. You cannot join it, but the record below documents what was studied.
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University of North Carolina, Chapel Hill