Clinical Trials Directory

Trials / Completed

CompletedNCT02932670

Minimum Effective Volume of Lidocaine Costoclavicular Brachial Plexus Block

Minimum Effective Volume of Lidocaine for Ultrasound-Guided Costoclavicular Infraclavicular Brachial Plexus Block

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to determine the minimum effective volume of lidocaine in 90% of patients (ED90) required for single-injection US-guided costoclavicular infraclavicular.

Detailed description

The aim of this study is to determine the minimum effective volume of lidocaine in 90% of patients (ED90) required for single-injection US-guided costoclavicular ICB. Determination of the minimum effective volume of LA is important because it prevents the administration of an unnecessarily large (and potentially toxic) dose. Furthermore, when multiple blocks need to be performed at the same time in the same patient, knowledge of the minimum effective volume allows to the operator to preserve efficacy without sacrificing safety for each block.

Conditions

Interventions

TypeNameDescription
OTHERcostoclavicular nerve blockultrasound-guided costoclavicular nerve block

Timeline

Start date
2016-10-01
Primary completion
2017-01-01
Completion
2017-02-01
First posted
2016-10-13
Last updated
2017-03-22

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02932670. Inclusion in this directory is not an endorsement.