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Navio With Total Knee Arthroplasty

NCT03317834 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 122

Last updated 2024-10-08

Study results available
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Summary

The purpose of this study is to demonstrate superior accuracy with the Navio ™ Robotic-assisted Surgical System in achieving desired post-operative mechanical alignment, compared to TKA procedures using standard instruments. An additional study purpose is to document clinical and patient-reported outcomes in subjects receiving TKA with the Navio ™ system.

Conditions

  • Total Knee Arthroplasty
  • Arthroplasty of Knee

Interventions

DEVICE

Navio ™ Robotic-assisted Surgical System

Total Knee Replacement

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Principal Investigators

  • Julie Lankiewicz · Smith & Nephew, Inc.

Eligibility

Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-13
Primary Completion
2018-10-25
Completion
2021-05-27
FDA Device
Yes

Countries

  • United States

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 NCT03317834 on ClinicalTrials.gov