MedTrace Logo

Maxim® Knee Pop-Top® Tibia vs. Regular Maxim® Knee Tibia

NCT00579059 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2017-07-17

Study results available
· View outcomes & findings →

Summary

The purpose of this prospective clinical data collection is to compare the outcomes of two different tibial bearings: the Maxim® Pop-Top® Tibia and Maxim® Modular Tibia.

Conditions

Interventions

DEVICE

Maxim® Knee System with Removable Molded Polyethylene Tibia

Used for total knee replacements

DEVICE

Regular Maxim® Knee System

Used for total knee replacements

Sponsors & Collaborators

  • Biomet Orthopedics, LLC

    lead INDUSTRY

Principal Investigators

  • Russell Wagner, MD · Harris Methodist Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-05-31
Primary Completion
2007-11-30
Completion
2007-11-30

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 NCT00579059 on ClinicalTrials.gov