RecruitingNot ApplicableNCT07818343

Hinge vs CCK Implants

A Randomized Controlled Trial Comparing Reoperation Rates and Clinical Outcomes of Rotating Hinge Versus Condylar Constrained Knee Implants in Revision Total Knee Arthroplasty


Sponsor

Medstar Health Research Institute

Enrollment

186 participants

Start Date

Feb 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The primary purpose of this study is to compare reoperation rates for rotating hinge knee implants versus condylar constrained knee implants when used in revision total knee arthroplasty. The secondary purposes are to compare patient satisfaction, loosening rates and clinical outcomes for RHK implants compared to CCK implants in rTKA. Additionally, knee range of motion and stability will be assessed and compared at all follow-up time points. We hypothesize that RHK implants provide patients undergoing rTKA with similar reoperation rates to those of patients who receive a CCK implant. The investigators hypothesize that patients who receive an RHK implant will have similar loosening rates and clinical outcomes compared to patients who receive a CCK implant. Lastly, knee stability and patient satisfaction may improve with the use of a rotating hinge device.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Condylar Constrained knee system. ( NexGen Legacy Condylar Constrained Knee by Zimmer Biomet) and a medical device called Rotating Hinge Knee ( NexGen Rotating Hinge Knee by Zimmer Biomet) for people with knee and revision arthroplasty. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years to 80 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICECondylar Constrained knee system. ( NexGen Legacy Condylar Constrained Knee by Zimmer Biomet)

Patients in this group will receive a condylar constrained knee implant at the time of surgery and will have their outcomes with this implant assessed over 10 years.

DEVICERotating Hinge Knee ( NexGen Rotating Hinge Knee by Zimmer Biomet)

Patients in this group will receive a rotating hinge knee implant and will be followed for the next 10 years to asses outcomes.


Locations(2)

Medstar Georgetown University Hospital

Washington D.C., District of Columbia, United States

Medstar Montgomery Medical Center

Olney, Maryland, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07818343


Related Trials