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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.
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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
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108 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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