Trials / Unknown
UnknownNCT02210429
Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of Single Shot Catheter Techniques
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Ann & Robert H Lurie Children's Hospital of Chicago · Academic / Other
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Not accepted
Summary
We hypothesize that patients who receive a supraclavicular block via Angiocath, placed intra-operatively and dosed post-operatively following neurologic examination, will have lower pain scores, lower use of intravenous morphine equivalents in the post-anesthesia care unit, and lower rates of intervention for post-operative nausea and vomiting. We also hypothesize that patients receiving this nerve block had the same rates of nerve damage as the patients who did not receive a block and that there will be no demonstrable safety concerns with this block.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Elbow Fracture Fixation |
Timeline
- Start date
- 2009-01-01
- Primary completion
- 2014-06-01
- Completion
- 2015-11-01
- First posted
- 2014-08-06
- Last updated
- 2015-07-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02210429. Inclusion in this directory is not an endorsement.