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Randomized Fixed Bearing vs Mobile Bearing Cruciate Retaining TKA

NCT00289094 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 99

Last updated 2022-09-13

Study results available
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Summary

The purpose of this study is to evaluate the clinical performance of the rotating platform and fixed bearing implants in patients undergoing primary total knee replacement. Outcome scoring and radiographic assessment will be the methods used to evaluate performance.

Conditions

Interventions

DEVICE

Total Knee Replacement

Rotating Platform (RP) Cruciate Retaining Knee System

DEVICE

Total knee replacement

Fixed Cruciate Retaining Knee System

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Principal Investigators

  • Tammy L O'Dell, EMT, CCRA, CCRC · 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
2001-03-01
Primary Completion
2007-12-26
Completion
2007-12-26
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT00289094 on ClinicalTrials.gov