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
| Type | Name | Description |
|---|---|---|
| OTHER | intermediate-acting digital nerve block | non-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.