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LPS Flex Porous Femoral Components

NCT01462240 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2021-08-24

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

LPS Flex Porous Femoral Components

Porous femoral components in total knee arthroplasty

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Kacy Arnold, RN, MBA · Zimmer Biomet

Eligibility

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

Timeline & Regulatory

Start
2008-05-20
Primary Completion
2012-03-31
Completion
2012-03-31

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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 NCT01462240 on ClinicalTrials.gov