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NCT06782295 · ClinicalTrials.gov registry record · Phase 4
The Use of CCK vs PS in Revision TKAs
A Phase 4 study of Aseptic Loosening of Prosthetic Joint and Instability of Prosthetic Joint, sponsored by Rush University Medical Center.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 170
- Enrollment target
- 1
- Study location
NCT06782295 is a Phase 4 study of Aseptic Loosening of Prosthetic Joint and Instability of Prosthetic Joint that is actively recruiting participants, run by Rush University Medical Center. The registered enrollment target is 170 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06782295, a Phase 4 study of Aseptic Loosening of Prosthetic Joint and Instability of Prosthetic Joint, is actively recruiting participants, sponsored by Rush University Medical Center.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 170 participants
- Enrollment target
- 1
- Study location
Study Summary
This study aims to compare the clinical impact of Constrained Condylar versus Posterior Stabilized Knee (PS) bearings on patient satisfaction and surgical outcomes including mid-term survivorship among patients undergoing revision total knee arthroplasty.
Conditions Studied
Interventions
- DEVICE Constrained Condylar bearing
- DEVICE posterior stabilized bearing
Study Locations (1)
Illinois
- Rush University Medical Center - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 170 participants |
| Start Date | 2025-07-01 |
| Est. Completion | 2038-07-01 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06782295
The ClinicalTrials.gov registry entry for NCT06782295 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 170 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rush University Medical Center, which has 320 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Aseptic Loosening of Prosthetic Joint appearing as the primary indexed condition, and to 2 interventions - of which Constrained Condylar bearing is the first listed.
NCT06782295 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT06782295 about?
NCT06782295 is a clinical study titled "The Use of CCK vs PS in Revision TKAs". This study aims to compare the clinical impact of Constrained Condylar versus Posterior Stabilized Knee (PS) bearings on patient satisfaction and surgical outcomes including mid-term survivorship among patients undergoing revision total knee arthroplasty.
What is the current status of trial NCT06782295?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 170 participants. The study started on 2025-07-01. Estimated completion is 2038-07-01.
What conditions does trial NCT06782295 study?
This clinical trial studies the following conditions: Aseptic Loosening of Prosthetic Joint, Instability of Prosthetic Joint, Reimplantation for Periprosthetic Joint Infection, Femoral Revision Indicated, Tibial Component Revision.
What interventions are being tested in trial NCT06782295?
The interventions under investigation include: Constrained Condylar bearing (DEVICE), posterior stabilized bearing (DEVICE).
Who is sponsoring clinical trial NCT06782295?
This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06782295 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Aseptic Loosening of Prosthetic Joint
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Instability of Prosthetic Joint
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