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Rejuvesol® Washed RBC in Sickle Cell Patients Requiring Frequent Transfusions

Primary Purpose

Sickle Cell Disease

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Rejuvesol
Blood transfusion
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Sickle Cell Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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%.

Sites / Locations

  • University of North Carolina at Chapel Hill
  • Duke Univeristy Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Transfusion with rejuvenated red blood cells (RBCs)

Transfusion with standard red blood cells

Arm Description

Subjects with sickle cell disease will receive RBCs treated with Rejuvesol®. Scheduled red cell exchanges performed with the last 4 units of the exchange having been incubated with Rejuvesol® solution. Only transfusions necessary for the treatment of the sickle cell disease will be given for the purpose of the study.

Subjects with sickle cell disease will receive standard RBCs. Only transfusions necessary for the treatment of the sickle cell disease will be given for the purpose of the study.

Outcomes

Primary Outcome Measures

Average Percent Hemoglobin (HbA) Decrement Per Day
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 Outcome Measures

Actual HbA Decrement (g/dl) With Indexing to Calculated Circulating Blood Volume
Actual HbA Decrement (g/dl) Without Indexing to Calculated Circulating Blood Volume
Change in RBC Microparticles (MP) Counts
Change in RBC/RBC-MP-mediated Thrombin Generation
Change in p50 Pre- and Post-transfusion

Full Information

First Posted
April 2, 2016
Last Updated
December 31, 2018
Sponsor
Duke University
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1. Study Identification

Unique Protocol Identification Number
NCT02731157
Brief Title
Rejuvesol® Washed RBC in Sickle Cell Patients Requiring Frequent Transfusions
Official Title
Rejuvesol® Washed RBC in Sickle Cell Patients Requiring Frequent Transfusions
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
December 2016 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sickle Cell Disease

7. Study Design

Primary Purpose
Other
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Transfusion with rejuvenated red blood cells (RBCs)
Arm Type
Experimental
Arm Description
Subjects with sickle cell disease will receive RBCs treated with Rejuvesol®. Scheduled red cell exchanges performed with the last 4 units of the exchange having been incubated with Rejuvesol® solution. Only transfusions necessary for the treatment of the sickle cell disease will be given for the purpose of the study.
Arm Title
Transfusion with standard red blood cells
Arm Type
Active Comparator
Arm Description
Subjects with sickle cell disease will receive standard RBCs. Only transfusions necessary for the treatment of the sickle cell disease will be given for the purpose of the study.
Intervention Type
Drug
Intervention Name(s)
Rejuvesol
Intervention Type
Procedure
Intervention Name(s)
Blood transfusion
Intervention Description
Only transfusions necessary for the treatment of the sickle cell disease will be given for the purpose of the study.
Primary Outcome Measure Information:
Title
Average Percent Hemoglobin (HbA) Decrement Per Day
Description
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.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Actual HbA Decrement (g/dl) With Indexing to Calculated Circulating Blood Volume
Time Frame
6 months
Title
Actual HbA Decrement (g/dl) Without Indexing to Calculated Circulating Blood Volume
Time Frame
6 months
Title
Change in RBC Microparticles (MP) Counts
Time Frame
6 months
Title
Change in RBC/RBC-MP-mediated Thrombin Generation
Time Frame
6 months
Title
Change in p50 Pre- and Post-transfusion
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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%.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ian J Welsby, BSc MBBS
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jay Raval, MD
Organizational Affiliation
University of North Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
Country
United States
Facility Name
Duke Univeristy Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States

12. IPD Sharing Statement

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Rejuvesol® Washed RBC in Sickle Cell Patients Requiring Frequent Transfusions

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