← Back to all trials
Completed
NCT02210429
Supraclavicular Blocks for Post-Operative Pain Control in Supracondylar Fracture Fixation, a Retrospective Analysis of Single Shot Catheter Techniques
Conditions: Acute Pain, Pain, Postoperative
Sex: All
Ages: N/A – 17 Years
Healthy volunteers: No
Enrollment: 200
Sponsor: Ann & Robert H Lurie Children's Hospital of Chicago
Location: Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois
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.
Eligibility Criteria
Inclusion Criteria:
* Age under 18
* Undergoing supracondylar fracture fixation in operating room
Exclusion Criteria:
* Incomplete or inaccessable chart data
Source: ClinicalTrials.gov (NCT02210429). StuddyBuddy aggregates publicly available trial information.