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Comparative Accuracy of Three Versions of Non-Invasive Hemoglobin Monitoring

Blood Loss Clinical Trial

Official title:
Comparative Accuracy of Three Versions of Non-Invasive Hemoglobin Monitoring.

Clinical Trial Summary

There is no study hypothesis. The purpose of this study is to compare the accuracy of the: 1) SpHb (Radical 7 Pulse Co-Oximetry with SpHb™) RevF sensor (currently marketed), 2) the SpHb RevG sensor (a new, limited release version), and 3) the Pronto-7 sensor (currently marketed version) in patients undergoing spine surgery.

Clinical Trial Description

The purpose of this study is to compare the accuracy of the: 1) SpHb RevF sensor (currently marketed), 2) the SpHb RevG sensor (a new, limited release version), and 3) the Pronto-7 sensor (currently marketed version) in patients undergoing spine surgery. The results from the three sensors will be compared to a blood hemoglobin level taken intermittently (as a function of the patient's anesthesia care) and analyzed in the UCSF Clinical Laboratories.

This is an observational study. ;

Study Design

Observational Model: Cohort

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01604668
Study type Observational
Source University of California, San Francisco
Contact
Status Completed
Phase N/A
Start date May 2012
Completion date May 2013
View Details
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