About this trial
This prospective observational cohort study aims to evaluate the association between perioperative dexamethasone administration and early postoperative recovery following primary total knee arthroplasty. In routine clinical practice, dexamethasone may be administered orally, intravenously, or not administered, depending on the surgeon's established perioperative protocol.
The primary objective is to assess early postoperative recovery in terms of pain intensity, functional mobility, and knee joint range of motion. Secondary objectives include evaluation of inflammatory response, postoperative metabolic changes, opioid requirement, and the severity of postoperative nausea and vomiting (PONV).
Group allocation is non-randomized and determined solely by the standard perioperative management approach routinely applied by the surgeon selected by the patient. No additional interventions are introduced for research purposes. All outcomes are assessed prospectively during the early postoperative period.
Eligibility criteria
Qualifiers
Age between 50 and 80 years
Diagnosis of primary knee osteoarthritis (primary gonarthrosis)
Scheduled for elective primary total knee arthroplasty
ASA physical status I or II
Disqualifiers
Revision total knee arthroplasty
History of knee joint infection
Inflammatory arthritis (e.g., rheumatoid arthritis)
Chronic systemic corticosteroid use
Trial design
Treatments tested in this trial
- Routine perioperative management
Treatment groups
Locations
1Sponsors and collaborators
Haseki Training and Research Hospital
Lead sponsor