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A Study to Compare the NexGen LPS and LPS-Flex Knee Implants

NCT00763386 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 331

Last updated 2012-06-04

Study results available
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Summary

The purpose of this study is to test for significant differences in functional outcomes obtained by using a NexGen LPS versus a NexGen LPS-Flex knee implant. Specifically, it is predicted that an increase in postoperative range of motion will be experienced by patients treated with the NexGen LPS-Flex knee implant.

Conditions

Interventions

DEVICE

NexGen LPS-Flex Fixed Bearing Knee

NexGen LPS-Flex Fixed Bearing femoral component

DEVICE

NexGen Legacy Posterior Stabilized Knee

NexGen Legacy Posterior Stabilized femoral component

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-06-30
Primary Completion
2009-12-31
Completion
2010-03-31

Countries

  • United States
  • Canada

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 NCT00763386 on ClinicalTrials.gov