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.