ARVIS TKA vs Conventional TKA
ConditionOsteoarthritis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorFoundation for Orthopaedic Research and Education
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
Patients with a previous operation of the same knee, including ACL reconstruction, fracture fixation, previous arthroplasty.
Patients that had a conversion to a different procedure intraoperatively or shortly after the TKA.
Diagnosed with greater than Killgren Lawrence Grade II OA on the contralateral knee
Patients that did not complete the TKA.
Trial design
Treatments tested in this trial
- Evaluation of Augmented Reality technology in TKA compared to standard TKA
Treatment groups
50 Participants
are divided into 2 treatment groupsSponsors and collaborators
Foundation for Orthopaedic Research and Education
Lead sponsor
DonJoy Orthopedics
Collaborator
Source ClinicalTrials.gov