Clinical Trials Directory

Trials / Completed

CompletedNCT01604668

Comparative Accuracy of Three Versions of Non-Invasive Hemoglobin Monitoring

Comparative Accuracy of Three Versions of Non-Invasive Hemoglobin Monitoring.

Status
Completed
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2012-05-01
Primary completion
2013-05-01
Completion
2013-05-01
First posted
2012-05-24
Last updated
2013-08-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01604668. Inclusion in this directory is not an endorsement.