Trials / Completed
CompletedNCT02287142
Evaluation of Supraclavicular, Suprascapular, and Interscalene Nerve Blocks for Outpatient Shoulder Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 189 (actual)
- Sponsor
- Benaroya Research Institute · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to assess analgesic efficacy of a supraclavicular nerve block, suprascapular nerve block, or interscalene nerve block in a population undergoing shoulder arthroscopy with rotator cuff repair. The investigators hypothesize that subjects from all three arms will receive equal analgesia since these blocks are routinely performed to treat post-operative pain after shoulder surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Brachial plexus nerve block | All arms of the study comparing the three different blocks are receiving the same single injection bolus of ropivacaine 0.5% prior to surgery. We will then record and compare pain scores in PACU and opioid requirement. |
Timeline
- Start date
- 2014-10-01
- Primary completion
- 2016-11-01
- Completion
- 2016-11-01
- First posted
- 2014-11-10
- Last updated
- 2017-02-02
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02287142. Inclusion in this directory is not an endorsement.