Clinical Trials Directory

Trials / Completed

CompletedNCT01226498

Effects of Blood Transfusion in Healthy Volunteers

Effects of Duration of Stored Red Blood Cell Transfusion on Physiological Parameters and Inflammatory Mediators in Healthy Adult Volunteers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Massachusetts General Hospital · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to assess effects of the storage of PRBC on endothelial function, inflammation and platelet activation in healthy volunteers

Detailed description

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

Conditions

Interventions

TypeNameDescription
PROCEDURERed blood Cells auto-transfusionWithdrawal from 10 Healthy volunteers of one unit of red blood cells and auto-transfusion after 3 days for one arm of the study, after 40 days for the other. Participants are enrolled in both arms of the study.

Timeline

Start date
2010-07-01
Primary completion
2010-11-01
Completion
2011-02-01
First posted
2010-10-22
Last updated
2014-01-30

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01226498. Inclusion in this directory is not an endorsement.