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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

TypeNameDescription
PROCEDUREElbow 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.

Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of S (NCT02210429) · Clinical Trials Directory