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WithdrawnNCT00850369Updated Jul 29, 2013

A Pilot Study of Chronic Red Blood Cell Transfusion in Sickle Cell Disease-Associated Pulmonary Hypertension

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 Withdrawn.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

Why this study was withdrawn
Slow accrual onto the study
Phase
Phase 2
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Pulmonary Hypertension
  • Sickle Cell Disease

Keywords

  • Pulmonary hypertension
  • Sickle cell disease
03

In context

Hypertension, Pulmonary

1,105 studies on the registry are indexed under Hypertension, Pulmonary; 234 are open to participants now.

Browse Hypertension, Pulmonary studies →

Lead sponsor

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.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. diagnosis of sickle cell anemia (HbSS) and HbSbeta0 thalassemia;
  2. male and female subjects between 18 and 65 years;
  3. documented PHT, but with pulmonary artery systolic pressures >/= 45 mmHg (TR jet velocity of >/= 3.0 m/s) on at least 2 separate visits at least 1 month apart;
  4. ability to give written informed consent to participate in the study; and
  5. in non-crisis steady state at time of enrollment

Exclusion criteria

Exclusion Criteria:

  1. treatment with epoprostenol (flolan) or similar prostacyclin analog, bosentan or sildenafil (or similar phosphodiesterase 5 inhibitor)
  2. on chronic anticoagulation
  3. RBC transfusion in previous 90 days;
  4. use of hydroxyurea
  5. multiple red cell alloantibodies that will make transfusion unsafe;
  6. baseline ferritin level > 1000 mg/dL
  7. pregnancy, and/or any condition which in the opinion of investigator might make the subject unsuitable for the study;
  8. patients with WHO functional class IV
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    1

    All subjects wil receive monthly RBC transfusions for 6 months

    Other: RBC transfusion

Interventions

  • OtherRBC transfusion

    Study subjects will receive monthly transfusions with 2 units of red blood cells

06

What researchers measure

Primary outcomes

  1. Pulmonary artery systolic pressure (mm Hg)

    Time frame: 2 years

  2. Pulmonary vascular resistance (dyne.s.cm-5)

    Time frame: 2 years

Secondary outcomes

  1. Six-minute walk

    Time frame: 2 years

  2. Markers of thrombin generation (TAT complexes, F1.2, d-dimers)

    Time frame: 2 years

  3. Markers of platelet activation (soluble CD40 ligand, beta thromboglobulin, platelet factor

    Time frame: 2 years

  4. Nitric oxide metabolites

    Time frame: 2 years

  5. Quality of life

    Time frame: 2 years

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00850369
Lead sponsor
University of North Carolina, Chapel Hill
Collaborators
Duke University
Responsible party
Sponsor
First posted
Feb 25, 2009
Start date
Feb 2005
Primary completion
May 2011
Completion
May 2011
Last update
Jul 29, 2013

Study contacts

Kenneth I Ataga, MD
principal investigator · University of North Carolina, Chapel Hill

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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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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