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Clinical Trial Summary

Patients scheduled to have a surgery for Total Knee Arthroplasty will be assigned to one of three groups, each group will use a different approach using the ultrasound to guide the femoral nerve block as part of their treatment for controlling pain post-operatively.


Clinical Trial Description

This will be a prospective, single-blinded, randomized study. The patients will be randomly assigned to one of three groups:

Group I - single shot femoral nerve block Group II - continuous femoral nerve block - non stimulating catheter Group III - continuous femoral nerve block - stimulating catheter ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01763814
Study type Interventional
Source Chicago Anesthesia Pain Specialists
Contact
Status Completed
Phase N/A
Start date December 2011
Completion date April 2019

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