MedTrace Logo

Primary TKA Cruciate Retaining vs Cruciate Substituting With Rotating Platform Knee Prostheses

NCT00289081 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 399

Last updated 2014-05-13

No results posted yet for this study

Summary

The purpose of the study is to evaluate the clinical performance of the cruciate ligament retaining or cruciate ligament substituting implants by obtaining a series of primary TKAs. 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 implant

DEVICE

Total knee replacement

Rotating Platform (RP) Cruciate Substituting Knee implant.

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Principal Investigators

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

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2001-02-28
Primary Completion
2006-06-30
Completion
2006-06-30

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 NCT00289081 on ClinicalTrials.gov