Effect of Low Dose Corticosteroids on Perioperative Markers of Thrombosis and Fibrinolysis in Total Knee Arthroplasty
Total Knee Arthroplasty
About this trial
This is an interventional treatment trial for Total Knee Arthroplasty focused on measuring Orthopedic Procedures, Prostheses and Implants, Joint Prosthesis, Knee Prosthesis, Arthroplasty, Knee, Thromboembolism, Inflammation, B-Cell Differentiation Factor-2, Differentiation Factor-2, B-Cell, B-Cell Stimulatory Factor-2, BSF-2, IFN-beta 2, MGI-2, Interleukin-6 (IL-6), Steroids, Pregnenediones, Hydrocortisone, Physiological Effects of Drugs, Therapeutic Uses
Eligibility Criteria
Inclusion Criteria:
- All patients undergoing unilateral or bilateral total knee replacement
- Age 50-90
Exclusion Criteria:
- All patients on steroid therapy regardless of dose or duration of treatment or those requiring stress-dose steroids preoperatively
- Patients who are smokers
- Patients under 50 years of age
- Patients over 90 years of age
- Patients with diabetes
- Patients with a prior history of corticosteroid intolerance
- Patients with previous complications of steroid use
Sites / Locations
- Hospital for Special Surgery
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Active Comparator
Placebo
Treatment
Patients receive a saline placebo before surgery, 8 hours after the first dose and 16 hours after the first dose.
Patients receive 3 100 mg of hydrocortisone: prior to surgery, 8 hours after the first dose and 16 hours after the first dose.