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Clinical Trial Summary

The researchers are trying to determine pain medication consumption in the first 24 hours after surgery in patients given the standard continuous infusion of local anesthetic versus patients given the same total dose via programmed intermittent dosing. Both groups will receive the option of patient controlled pain medication as well as the same dose of pre-programmed pain medication. The only difference is the rate of administration: continuous vs. hourly intervals.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03480984
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase N/A
Start date February 5, 2018
Completion date January 31, 2020

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