Clinical Trials Directory

Trials / Completed

CompletedNCT01075620

Comparison of Nonposterior- and Posterior-Stabilized Mobile-Bearing Total Knee Arthroplasty

Comparison of Nonposterior- and Posterior-Stabilized Mobile-Bearing Total Knee Arthroplasty A Prospective, Randomized Study

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
126 (actual)
Sponsor
Ewha Womans University · Academic / Other
Sex
All
Age
30 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if there are any clinical or radiographic differences in non-posterior stabilized rotating mobile bearing design versus a posterior stabilized rotating mobile bearing designs.

Detailed description

Out comes measures were to determine 1. whether the knee and function scores and the radiographic results of the knees with a PFC Sigma RP knee prosthesis would be better than those with an LCS RP prosthesis. 2. whether the patients with a PFC RP knee prosthesis would have a better range of knee motion than those with an LCS RP prosthesis. 3. whether patient satisfaction and preference would be better in the patients having a PFC Sigma RP knee prosthesis than those of patients having an LCS RP knee prosthesis 4. whether complication rate would be less in the knees with a PFC sigma RP knee prosthesis than in the knees with an LCS RP prosthesis.

Conditions

Interventions

TypeNameDescription
DEVICEPFC-Sigma RPPosterior stabilizing rotating platform total knee components
DEVICELPS RPnon-posterior stabilized rotating platform design

Timeline

Start date
2002-05-01
Primary completion
2002-12-01
Completion
2010-01-01
First posted
2010-02-25
Last updated
2010-02-25

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01075620. Inclusion in this directory is not an endorsement.