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Clinical Trial Summary

The purpose of this study is to prospectively compare post-operative pain relief in pediatric patients undergoing traumatic femur fracture repair who have received either a femoral nerve block with a lateral femoral cutaneous nerve block or a standard anesthetic for analgesia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01759407
Study type Interventional
Source Nationwide Children's Hospital
Contact
Status Terminated
Phase Phase 2
Start date May 2013
Completion date October 2016