Clinical Trials Directory

Trials / Completed

CompletedNCT01750554

The Influence of a Bupivacaine Digital Nerve Block Using Rev G.

The Influence of a Bupivacaine Digital Nerve Block With the New Continuous Sensor (Rev G) on the Accuracy of SpHb Monitoring.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
19 (actual)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The investigators are proposing to continue investigation to improve the accuracy of the SpHb (continuous hemoglobin monitoring device) by administering an intermediate acting digital nerve block in the finger connected to the SpHb, specifically bupivacaine 0.25% in patients undergoing spine surgery. Bupivacaine is FDA approved and in routine use.

Detailed description

Patients undergoing spine surgery will be randomized to receive (or not) the bupivacaine digital block on the finger attached to the new limited release version of the hemoglobin sensor, RevG. The SpHb reading will be compared to a blood hemoglobin level analyzed in the UCSF Clinical Laboratories.

Conditions

Interventions

TypeNameDescription
OTHERintermediate-acting digital nerve blocknon-therapeutic Bupivacaine digital nerve block to assess effect on accuracy of diagnostic readings

Timeline

Start date
2012-12-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2012-12-17
Last updated
2015-04-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01750554. Inclusion in this directory is not an endorsement.