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Post-op Prednisone and Glucose Monitoring in TKA

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Eligibility criteria expanded, about 35 words
  2. Recruitment opened Start date changed from estimate of Jul 1, 2026 to Jun 22, 2026 · Eligibility criteria expanded, about 8 words · Site details revised Show 3 more changesShow less
    • Start date changed from estimate of Jul 1, 2026 to Jun 22, 2026
    • Eligibility criteria expanded, about 8 words
    • Site details revised
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study compares the efficacy of a 5-day post-operative oral prednisone regimen (40 mg daily) with the standard intraoperative steroid regimen, focusing on pain, swelling, range of motion, opioid use, and glucose levels monitored continuously.
Trial Details
NCT Number NCT07630896
Lead Sponsor Columbia University
Collaborators: Orthopaedic Scientific Research Foundation
Conditions Osteoarthritis, Unicompartmental Knee Arthroplasty, Total Hip Arthroplasty (THA)
Enrollment 104 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov