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Clinical Trials/NCT00954954
NCT00954954
Completed
Phase 4

Outcomes After Standard and High-Flexion Posterior Stabilized Rotating-Platform Mobile-Bearing Total Knee Arthroplasty: A Prospective Randomized Comparative Study

Seoul National University Hospital1 site in 1 country170 target enrollmentOctober 2006

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Osteoarthritis, Knee
Sponsor
Seoul National University Hospital
Enrollment
170
Locations
1
Primary Endpoint
Range of knee motion, knee scores, patients' abilities to perform deep knee flexion related activities, patient satisfaction and radiographic indices were measured.
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The aim of this prospective study is to compare the clinical and radiographic outcomes of standard and high-flexion posterior stabilized (PS) rotating-platform mobile-bearing (RP-MB) total knee arthroplasty. The investigators hypothesize that total knee arthroplasty performed with a high-flexion PS RP-MB design would improve range of motion, and that this would be reflected by a better clinical outcome and greater patient satisfaction.

Detailed Description

A high-flexion, PS RP-MB prosthesis was designed to improve range of motion after total knee arthroplasty without compromising the theoretical advantages of the standard PS RP-MB system. To date, no study has prospectively compared the clinical and radiographic results of standard and high-flexion PS RP-MB designs.

Registry
clinicaltrials.gov
Start Date
October 2006
End Date
July 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • A diagnosis of primary osteoarthritis of knee
  • A candidate for total knee replacement arthroplasty

Exclusion Criteria

  • A diagnosis other than primary osteoarthritis
  • A history of previous open knee surgery

Outcomes

Primary Outcomes

Range of knee motion, knee scores, patients' abilities to perform deep knee flexion related activities, patient satisfaction and radiographic indices were measured.

Time Frame: 2 years

Study Sites (1)

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