Pain Management Clinical Trial
Official title:
Evaluation of Post Hospital Administration of Celecoxib Following Minimally Invasive Knee Replacement Surgery: A Randomized Controlled Study
This study will evaluate the benefits of continuing celecoxib through six weeks of total
knee arthroplasty recovery. This is a randomized, double blind study with a group of
approximately 130 primary total knee patients. All patients will receive celecoxib
throughout their hospitalization as per current minimally invasive total knee arthroplasty
protocol. At the time of hospital discharge, participating patients will be randomly placed
on either celecoxib 200mg twice a day or a placebo twice a day.
This study will determine if the continued use of celecoxib for six weeks after total knee
arthroplasty hospitalization will further decrease narcotic consumption, improve knee range
of motion, improve ambulatory ability, and improve patient satisfaction over patients
receiving celecoxib only during the acute hospitalization.
n/a
Observational Model: Cohort, Time Perspective: Prospective
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