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Feasibility Study of Mirasol-Treated Whole Blood Red Cell Recovery and Survival — IMPROVE  

Healthy Clinical Trial

Official title:
IMPROVE: Inactivation of Whole Blood With Mirasol (R): Performance in Red Blood Cells, Platelets and Plasma Investigation

Clinical Trial Summary

Feasibility trial to evaluate recovery and survival of red blood cells (RBCs) from Mirasol-treated whole blood

Clinical Trial Description

Radiolabeling of red blood cells (RBCs) followed by infusion back to the donor is commonly used to test the quality of RBCs in a person. By measuring the level of radioisotope in a blood sample, these tests evaluate what percentage of the RBCs remain in the bloodstream after 24 hours (recovery) and can predict how long the RBCs will remain in circulation (survival). The IMPROVE trial is a feasibility trial to evaluate these parameters in RBCs obtained from whole blood units that have been treated with the Mirasol System. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00742001
Study type Interventional
Source Terumo BCTbio
Contact
Status Terminated
Phase Phase 1
Start date September 10, 2008
Completion date December 16, 2008
View Details
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