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Completed

NCT Number: NCT02731157

Rejuvesol® Washed RBC in Sickle Cell Patients Requiring Frequent Transfusions

The objective of this proposal is to test the feasibility of red blood cell (RBC) rejuvenation to chronic transfusion in sickle cell disease (SCD) and the potential benefit of RBC rejuvenation in this population to determine if a larger clinical trial powered to definitively characterize the benefits of rejuvenation is warranted.

This is a small pilot study is to see if restoring important energy molecules (ATP and 2,3,DPG) in stored red blood cells before they are transfused, with a rejuvenating solution (Rejuvesol), offers any advantages to individuals over standard blood transfusion. Subjects will receive either rejuvenated (R) or standard (S) RBCs with each transfusion for 6 transfusions (over approximately a 6-month period) in a pre-defined order to maximize detection of any signal.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States

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About this study

Blood transfusion is part of the standard care for individuals that have sickle cell disease. Often these transfusions become needed quite frequently. The purpose of the red blood cells in the blood is to deliver oxygen to the organs and tissues of the body. People with sickle cell disease have abnormal red blood cells. Stored blood undergoes some changes that may make it less effective in achieving this goal.

The purpose of this study is to see if restoring important energy molecules (ATP and 2,3,DPG) in stored red blood cells before they are transfused, with a rejuvenating solution (Rejuvesol), offers any advantages to individuals over standard blood transfusion. This is a Food and Drug Administration (FDA) approved process that is described by the American Association of Blood Banks for prolonging blood storage but not used for everyday transfusions. The investigators want to use this process to improve blood transfused to individuals who need frequent transfusions. Potential advantages include better delivery of oxygen by the transfused red blood cells and easier release of oxygen to the tissues. In addition the study will assess how using the rejuvenated blood affects the interval between transfusions. This means possibly that transfusions may not be needed as often.

Although Rejuvesol has been previously approved by the FDA, it is not routinely used to prepare standard blood transfusions to individuals who have sickle cell disease. Use of Rejuvesol in this study is considered investigational.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Stable, compliant, chronically transfused sickle cell disease (SCD) patients
  • Currently maintained crisis-free with repeated RBC therapy for at least 3 consecutive sessions
  • ≥18 years old
  • Have Hb SS disease
  • Have the capacity to give informed consent

Exclusion criteria

  • Baseline need for washed RBCs
  • Pre-treatment SaO2 < 92%.

Treatment and study plan

Rejuvesol

Drug

Blood Transfusion

Procedure

Only transfusions necessary for the treatment of the sickle cell disease will be given for the purpose of the study.

Primary outcomes

  1. Average Percent Hemoglobin (HbA) Decrement Per Day

    Time frame: 6 months

    The %HbA decrement is the current pre-treatment HbA - previous post treatment HbA in %. The average %HbA decrement per day was calculated using matched pairs.

Secondary outcomes

  1. Actual HbA Decrement (g/dl) With Indexing to Calculated Circulating Blood Volume

    Time frame: 6 months

  2. Actual HbA Decrement (g/dl) Without Indexing to Calculated Circulating Blood Volume

    Time frame: 6 months

  3. Change in RBC Microparticles (MP) Counts

    Time frame: 6 months

  4. Change in RBC/RBC-MP-mediated Thrombin Generation

    Time frame: 6 months

  5. Change in p50 Pre- and Post-transfusion

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Apr 7, 2016
Registry last updated
Jan 25, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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