Post-op Prednisone and Glucose Monitoring in TKA
- NCT ID
- NCT07630896
- Registry status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 4
- Sponsor
- Columbia University
- Conditions
- Osteoarthritis, Total Hip Arthroplasty (THA), Unicompartmental Knee Arthroplasty
Overview
ClinicalTrials.gov lists this study as Recruiting.
Official title: Postoperative Prednisone Regimen in TKA and Its Effect on Continuous Glucose Levels
Enrollment: 104 participants (Estimated).
What is being studied
- Device: Continuous Glucose Monitor
- Intervention: Fused-Ring Compounds
- Other: InkWell Health Tattoos
- Intervention: Polycyclic Compounds
- Intervention: Prednisone
- Drug: Prednisone
- Intervention: Pregnadienediols
- Intervention: Pregnadienes
- Intervention: Pregnanes
- Intervention: Steroids
Who may be eligible
- Ages
- 18 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Study locations
1 study location is listed.
Recruiting site status is explicitly provided for 1 location; 1 is listed as Recruiting.
Countries: United States
- New York, United States: 1
Sample of listed locations
- Columbia University Irving Medical Center — New York, New York, 10032, United States — Recruiting
Study details
- Start date
- June 22, 2026
- Primary completion date
- December 1, 2027
- Completion date
- March 1, 2028
- First posted
- June 5, 2026
- Collaborators
- Orthopaedic Scientific Research Foundation
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07630896
- Registry last updated
- October 2, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07630896 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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