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Recruiting NCT07630896

Post-op Prednisone and Glucose Monitoring in TKA

Conditions: Osteoarthritis, Unicompartmental Knee Arthroplasty, Total Hip Arthroplasty (THA)

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 104
Sponsor: Columbia University

Location: Columbia University Irving Medical Center New York New York

Summary

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.

Eligibility Criteria

Inclusion Criteria: * MUST BE CONTACTED BY THE STUDY TEAM TO BE PART OF THE STUDY. No applications taken * Undergoing Primary Unicompartmental Knee Arthroplasty or Total Hip Arthroplasty * Age 18 and above * Patient at Columbia University Irving Medical Center and be undergoing planned surgery by Dr. Roshan P. Shah Exclusion Criteria: * Steroid therapy * Narcotic use within past 3 months * History of corticosteroid intolerance * Pregnancy * Uncontrolled diabetes * Doesn't own smart phone Drop Criteria: \- 2nd dose of IV dexamethasone

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07630896). StuddyBuddy aggregates publicly available trial information.