Evaluation of Post Hospital Administration of Celecoxib Following Minimally Invasive Knee Replacement Surgery

• Status: Completed
• Trial end date: 2009-12-01
• Target enrollment: 0
• Participant gender: All

Summary

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.

Details

• Lead Sponsor: St. Louis Joint Replacement Institute
• Collaborators: Biomet, Inc.; Pfizer; Zimmer Biomet
• Treatments: Celecoxib

Criteria

Inclusion Criteria:

• having undergone a minimally invasive total knee by select surgeon

• voluntarily enrolled

• independent community ambulators

• only patients being discharged directly home

Exclusion Criteria:

• celecoxib allergy or intolerence

• Renal insufficiency (defined as serum creatine level >1.5 mg/dL or BUN level >22mg/dL

• History of bleeding gastic or duodenal ulceration

• New York Heart Association Class III or IV Congestive Heart Failure

• Previous myocardial infarction or cerebralvascular event

• Severe inflammatory bowel disease

• Known coagulation abnormality or hepatic disease

• Chronic coumadin administration

• Refusal by primary or cardiac physician