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Clinical Trial Summary

Consenting patients with proximal tibia fractures will be randomized to 10 degree or 21 degree cryotherapy sleeves. Time to discharge and complications will be monitored.

Primary outcome measure: Cost of Treatment (based on length of stay) Secondary outcome measures: Satisfaction/pain relief and narcotic requirement


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01104831
Study type Interventional
Source University of Manitoba
Contact
Status Terminated
Phase Phase 3
Start date April 2010
Completion date November 2012