Blood Transfusion, Autologous Clinical Trial
Official title:
Effects of Duration of Stored Red Blood Cell Transfusion on Physiological Parameters and Inflammatory Mediators in Healthy Adult Volunteers
The objective of this study is to assess effects of the storage of PRBC on endothelial function, inflammation and platelet activation in healthy volunteers
The objective of this study is to assess effects of the storage of PRBC on endothelial
function, inflammation and platelet activation in healthy volunteers.
The present study consists of two parts. During one phase of the study, 10 healthy human
volunteers will donate a unit of blood, which will be leukoreduced and stored in Additive
Solutions-1 (AS-1), and then transfused back to the subjects after 2 days of storage at 4º C
in the MGH Blood Bank. The other part of the study consists in the collection of a unit of
blood from the same volunteers, but which will be transfused back to the same subject after
40 days of storage. There will be a break of 2 week period in between these 2 study phases.
The order of these 2 study parts will be randomized.
We hypothesize that old red blood cells stored under conventional conditions may trigger a
complex, pro-inflammatory, pro-thrombotic and vasoconstriction response. We will compare the
response to PRBC stored for 2 days with the response to PRBC stored for 40 days in the same
healthy volunteers. We will monitor/measure the following markers/parameters:
1. Endothelium-mediated changes in vascular (arterial) tone
2. Tissue oxygen saturation will be continuously assessed during and after blood
transfusion
3. Hemolysis as quantified by changes in plasma haptoglobin level, plasma free hemoglobin,
LDH level, bilirubin level, iron level, ferritin, and transferrin
4. Changes of plasma and red blood cell levels of circulating nitrate, nitrite, RXNO,
RNNO, NO-heme
5. Concentration of cytokines, such as IL-6, IL-8, IL-10, IL-12, TNF, IFN-γ
6. Activation of platelets through circulating P-selectin expression on platelets
7. Activation of inflammatory lipid mediators
8. Changes in gene expression profiling analyzing RNA microarray of circulating leukocytes
;
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Basic Science
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03548766 -
Using DNA-Typing and Erythrocyte Microparticle Analysis to Detect Blood Doping
|
Phase 3 | |
Completed |
NCT00822588 -
Comparison in Need for Bank Blood Between Patients Undergoing Total Hip Surgery That Either Receive Their Own Blood Back or Not
|
N/A | |
Completed |
NCT00839241 -
A Clinical Study to Investigate if Transfusion of Patients Own Shed Blood Improves the Immunological Status in Comparison to Transfusion of Donor Blood ("Bank Blood")
|
N/A | |
Completed |
NCT00270075 -
A Study to Determine the Safety and Effectiveness of Epoetin Alfa in Facilitating Self-donation of Blood Before Surgery in Patients Who Are Not Anemic and Who Will be Undergoing Orthopedic or Heart and Blood Vessel Surgery
|
Phase 2/Phase 3 | |
Completed |
NCT02684747 -
Detecting Autologous Transfusion by Measuring Alterations in the Dynamics of Red Blood Cell Maturation and Recycling
|
Early Phase 1 | |
Completed |
NCT00270023 -
A Study to Determine the Effectiveness of Epoetin Alfa in Facilitating Self-donation of Blood Before Surgery in Non-anemic Patients Who Are Undergoing Orthopedic, Heart and Blood Vessel, or Breast Reduction Surgery; Performed in Combination With a Procedure to Reduce Blood Loss During Surgery.
|
Phase 2/Phase 3 |