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LEGION Hinge Safety and Efficacy Study

NCT02445443 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2024-11-27

No results posted yet for this study

Summary

The purpose of the current investigation is to assess the safety and efficacy of a new hinged revision knee device. This device is designed to provide efficient, reproducible reconstructions with optimal limb and implant alignment, durable implant fixation, and functional outcomes that increasingly approach those of primary Total Knee Arthroplasty (TKA).

Conditions

  • Knee Arthroplasty, Total

Interventions

DEVICE

LEGION Hinge Knee System

All enrolled/treated subjects will receive the LEGION Hinge Knee System.

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Eligibility

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

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2027-12-31
Completion
2028-08-01

Countries

  • United States
  • Australia
  • Belgium
  • Canada
  • Spain

Study Locations

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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 NCT02445443 on ClinicalTrials.gov