Trials / Completed
CompletedNCT01761175
Comparison of Ultrasound-Guided Infraclavicular Block and Ultrasound-Guided Axillary Block
Comparison of Ultrasound-Guided Single Injection Infraclavicular Block or Ultrasound-Guided Double Injection Axillary Block : A Non-inferiority Randomized Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 224 (actual)
- Sponsor
- CHU de Quebec-Universite Laval · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the rate of complete sensory block at 30 minutes following ultrasound-guided single injection infraclavicular block and ultrasound-guided double injection axillary block. The investigators research hypothesis is that both blocks will show comparable rates of complete sensory block at 30 minutes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Ultrasound-guided infraclavicular block | Ultrasound-guided single injection infraclavicular block: using an in-plane technique, 30 mL of mepivacaine 1.5% is injected at the posterior aspect of the artery. |
| PROCEDURE | Ultrasound-guided axillary block | Ultrasound-guided double injection axillary block: using an in-plane technique, 25 mL of mepivacaine 1.5% is injected postero-medial to the artery. During needle withdrawal, 5 mL of the same solution is injected close to the musculocutaneous nerve. |
Timeline
- Start date
- 2012-09-01
- Primary completion
- 2013-02-01
- Completion
- 2013-03-01
- First posted
- 2013-01-04
- Last updated
- 2017-08-04
- Results posted
- 2017-08-04
Locations
2 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT01761175. Inclusion in this directory is not an endorsement.