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
| Type | Name | Description |
|---|---|---|
| OTHER | costoclavicular nerve block | ultrasound-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.