Clinical Trials Logo

Knee Prosthesis clinical trials

View clinical trials related to Knee Prosthesis.

Filter by:

NCT ID: NCT01864434 Completed - Knee Prosthesis Clinical Trials

In Vivo Kinematics Comparison of Stryker or Zimmer Total Knee Arthroplasty

Start date: June 2013
Phase:
Study type: Observational

This study will compare the kinematics data collected from patients with implants created by different manufacturers to see which of these implants provides a more normal-like kinematic pattern compared to the normal knee.

NCT ID: NCT01714492 Completed - Knee Prosthesis Clinical Trials

Mechanics Analysis of Patients Having a Sigma Mobile Bearing TKA

Sigma MB TKA
Start date: April 2012
Phase:
Study type: Observational

Utilize previously developed mathematical model to determine in vivo knee mechanics (kinematics, forces, stresses, areas and sound) for subjects having a Sigma Posterior Stabilizing (PS) mobile bearing (MB) total knee arthroplasty (TKA). There are several hypotheses for this study, although the most prominent is: Subjects having a Sigma RP PS TKA will experience polyethylene bearing rotation at 10 years post-operative, similar to their previous evaluations at six months, two years and five years.

NCT ID: NCT01290640 Completed - Knee Arthroplasty Clinical Trials

Comparison of Kinematics for Subjects Implanted With a PFC Sigma Rotating Platform or Fixed Bearing TC3 Prosthesis

PFC & TC3
Start date: February 2011
Phase:
Study type: Observational

The objectives of this study are four-fold: 1. To determine the three-dimensional, in vivo kinematics for subjects having either a fixed- or mobile-bearing Press Fit Condylar (PFC) Sigma Total Condylar III Prosthesis, comparing the in vivo kinematics to determine if one implant type leads to a benefit for the patient. 2. To determine if bearing mobility occurs in PFC Sigma Rotating Platform Total Condylar III Prosthesis under in vivo, weight-bearing conditions during multiple activities (gait, stair descent, deep knee bend and chair rise). 3. To determine if there is a correlation between in vivo kinematic data obtained using fluoroscopy, electromyography (EMG) and ground reaction force (GRF) data and determine if variability occurs between these two TKA types. 4. To determine if a clinical benefit is either visibly detected (video camera) or quantifiably determined (questionnaire) for either TKA type.

NCT ID: NCT01290627 Completed - Knee Prosthesis Clinical Trials

In Vivo Determination of 3D Patellofemoral Mechanics

Patella
Start date: February 2011
Phase:
Study type: Observational

This study will analyze the tibio-femoral and patellofemoral (motion) and mechanics (forces) of participants having a normal knee or a total knee arthroplasty (TKA) using one or two different (TKA) devices Low Contract Stress (LCS) Posterior Stabilizing (PS) Rotating Platform (RP) Total Knee Arthroplasty (TKA). All knees will be analyzed using an image matching technique that will convert a two-dimensional (2D) fluoroscopic image into a three-dimensional (3D) image. In conjunction with the fluoroscopic analysis, electromyography (EMG) data, and ground reaction force (GRF) data will all be allow for a complete analysis of the knee joints. These results will help the orthopaedic community better understand knee motion so they can improve testing on existing implants and develop future implants that will further enhance patients' lives.