ARVIS Guidance vs Conventional Surgery for Knee Osteoarthritis

ARVIS TKA vs Conventional TKA

Recruiting N/A Interventional Study
Osteoarthritis
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
50 (estimated)
Sponsor
Foundation for Orthopaedic Research and Education · Other
Who this trial is looking for

This trial is looking for adults who need knee replacement surgery due to osteoarthritis. Participants will help test a new guidance system used during surgery to see if it improves outcomes.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am over 18 years old
  • I am scheduled for knee replacement surgery
  • I have osteoarthritis on the affected knee
  • I can provide informed consent

You may not be able to join if

  • I have had surgery on the same knee before
  • I had a different procedure during or shortly after my knee surgery
  • I have severe osteoarthritis on my other knee
  • I did not complete my knee surgery
  • The doctor thinks I cannot follow the study requirements

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

This study is a pilot analysis of a novel augmented reality guidance platform, the augmented reality visualization and information system (ARVIS, Insight Medical), with aims to demonstrate accuracy of bone resection and implant alignment during kinematic alignment total knee arthroplasty.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age over 18 years old * Scheduled for primary conventional TKA with kinematic alignment * Primary Diagnosis of Osteoarthritis (Killgren Lawrence Grade \> III) on affected side * Able to provide informed consent Exclusion Criteria: 1. Patients with a previous operation of the…
Contacts

Debbi Warren, RN

813-910-3688

dwarren@foreonline.org

CONTACT

Peter Simon

312-509-5761

psimon@foreonline.org

CONTACT