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

270 Participants
are divided into 3 treatment groups

Locations

1
Sultangazi Haseki Training and Research Hospital34200, IstanbulIstanbul, Turkey (Türkiye)

Sponsors and collaborators

Haseki Training and Research Hospital

Lead sponsor