Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611-2605, United States
NCT Number: NCT02210429
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.
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Notify MeUp to 17 year
All sexes
Observational
Chicago, Illinois, 60611-2605, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 24 hours
Total doses
Time frame: 24 hours
Total doses
Time frame: 1 month
Evaluated by surgeon at follow up.
Time frame: 24 hours
Using Visual Analog Scale and FLACC pain scale (for younger children) we will compare pain scores in the various groups.
Ann & Robert H Lurie Children's Hospital of Chicago
Other
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