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In Vivo Kinematics for Subjects Having a MicroPort Medial Pivot or DePuy Attune PCR TKA — TKA PCR  

Total Knee Arthroplasty Clinical Trial

Official title:
In Vivo Kinematics for Subjects Having a MicroPort Medial Pivot or DePuy Attune Posterior Cruciate Retainign Total Knee Arthroplasty

Clinical Trial Summary

In vivo knee kinematics will be assessed for 20 subjects that have been implanted with either a MicroPort Medial Pivot or DePuy Attune posterior cruciate retaining (PCR) total knee arthroplasty (TKA) by Dr. Russell Nevins of Nevada Orthopedic & Spine Center [this is the location from which participants will be recruited].

Clinical Trial Description

There will be ten subjects with the MicroPort implant and ten with the DePuy Attune implant; however, we will increase enrollment to 24 subjects (12 in each group) to ensure that researchers acquire the necessary 20 usable datasets for analysis and also to account for any subjects that may drop out of the study. All TKAs should be judged clinically successful based on the surgeon's evaluation and each patient's Forgotten Knee Score. Each subject should have a well-functioning prosthesis, be at least six months post-operative, and should have good-to-excellent post-operative passive flexion. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04103502
Study type Observational
Source The University of Tennessee, Knoxville
Contact Richard Komistek, Ph.D.
Phone 8659744159
Email rkomistek@aol.com
Status Not yet recruiting
Phase
Start date May 2024
Completion date December 2024
View Details
See also
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