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Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee

NCT00854295 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 266

Last updated 2023-02-14

Study results available
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Summary

The purpose of the study is to assess the long-term performance of the NexGen LPS-Flex Mobile Bearing Knee in the treatment of patients with severe knee pain or degenerative knee disease.

Conditions

  • Osteoarthritis
  • Traumatic Arthritis
  • Avascular Necrosis of the Femoral Condyle
  • Moderate Varus
  • Valgus
  • Flexion Deformities

Interventions

DEVICE

NexGen LPS-Flex Mobile Bearing Knee

Total Knee Replacement

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Erin Osborn · Zimmer Biomet

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-04-30
Primary Completion
2020-06-30
Completion
2021-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT00854295 on ClinicalTrials.gov