Clinical Trials Directory

Trials / Completed

CompletedNCT00956683

Dual Endpoint Nerve Stimulation Versus Ultrasound in Infraclavicular Block for Hand Surgery

A Randomized Controlled Study Comparing Dual Endpoint Nerve Stimulation With Ultrasound-guided Infraclavicular Block for Hand Surgery.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
106 (actual)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Current best practice for performance of infraclavicular block dictates the use of a dual-endpoint nerve stimulation technique that still only results in a 79% success rate. Use of an ultrasound-guided technique has the potential to significantly improve success. A randomized, controlled study to evaluate this area remains to be performed and is required to demonstrate to anesthesiologists that an ultrasound-guided approach should supersede nerve stimulation as the technique of choice for infraclavicular block.

Conditions

Interventions

TypeNameDescription
PROCEDUREUltrasound Guided Infraclavicular Nerve BlockUse of Ultrasound to help guide needle placement and local anesthetic injection during infraclavicular nerve block.
PROCEDUREDual-Endpoint nerve stimulationUse of dual-endpoint nerve stimulation to guide needle placement and local anesthetic injection during infraclavicular nerve block.

Timeline

Start date
2006-01-01
Primary completion
2008-08-01
Completion
2008-12-01
First posted
2009-08-11
Last updated
2009-08-11

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT00956683. Inclusion in this directory is not an endorsement.