LPS Flex Porous Femoral Components

Status Withdrawn

Clinical Trial Summary

This is a prospective multicenter study of the LPS-Flex Porous Femoral Components when used in primary total knee arthroplasty. The purpose of the study is to obtain short-, mid-, and long-term clinical outcomes and implant survivorship data for the NexGen LPS-Flex Porous Femoral components.

Clinical Trial Description

Survival and outcome data on the NexGen LPS-Flex Porous Femoral Components will be done by an analysis of standard scoring system, radiographs and adverse event records. Survivorship will be evaluated by monitoring the frequency and incidence of adverse events, serious adverse events, adverse device effects, serious adverse device effects, and unanticipated adverse device effects. Outcomes will be measured by comparing the overall pain and function performances (based on the Knee Society Scoring System), survivorship, subject quality of life and radiographic parameters of study subjects receiving the LPS-Flex Porous Femoral Components. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01462240
Study type	Observational
Source	Zimmer Biomet
Contact
Status	Withdrawn
Phase
Start date	May 20, 2008
Completion date	March 2012

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