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Randomized Fixed Bearing vs Mobile Bearing Cruciate Substituting TKA

NCT00289107 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 149

Last updated 2023-05-03

Study results available
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Summary

The study will evaluate the clinical performance of the rotating platform and fixed bearing implants through patient questionnaires, outcomes scoring and radiographic assessment.

Conditions

Interventions

DEVICE

Total Knee Arthroplasty

Rotating Platform (RP) Cruciate Substituting Knee System

DEVICE

Total knee replacement

Fixed Cruciate Substituting Knee System

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Tammy L O'Dell, EMT, CCRA · DePuy Orthopaedics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-04-01
Primary Completion
2007-11-01
Completion
2007-11-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00289107 on ClinicalTrials.gov