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ARVIS TKA vs Conventional TKA
A Prospective Study Using Augmented Reality Versus Conventional Jig Controls in Total Knee Arthroplasty for Osteoarthritis
Who can join
Ages 18 and older · All sexes
Full 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 same knee, including ACL reconstruction, fracture fixation, previous arthroplasty. 2. Patients that had a conversion to a different procedure intraoperatively or shortly after the TKA. 3. Diagnosed with greater than Killgren Lawrence Grade II OA on the contralateral knee 4. Patients that did not complete the TKA. 5. Patients the Investigator deems not able to follow through with study requirements such as follow-up visits or PROM's.
About the study
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.
What is being tested
- Evaluation of Augmented Reality technology in TKA compared to standard TKA (other)
Sponsor: Foundation for Orthopaedic Research and Education · Participants: 50 · Started: Dec 1, 2024
Contact the study team
- Debbi Warren, RN · Phone: 813-910-3688
- Peter Simon · Phone: 312-509-5761
Official record on ClinicalTrials.gov — NCT06663384
Locations in the U.S.
| Florida | Florida Orthopaedic Institute, Tampa |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.