ARVIS TKA vs Conventional TKA
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Evaluation of Augmented Reality technology in TKA compared to standard TKA.
- Who it may be relevant to
- Registry conditions: Osteoarthritis. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Prospective Study Using Augmented Reality Versus Conventional Jig Controls in Total Knee Arthroplasty for Osteoarthritis
Overview
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.
Detailed description
This study is a Randomized Controlled Trial evaluating the effectiveness of an AR system utilized to perform bone cuts when compared to traditional jigs in primary TKA for treatment of primary osteoarthritis. Our primary objective is to determine if the ARVIS augmented reality platform is a reliable tool to restore native lower extremity alignment during TKA. An estimated 50 patients will be enrolled in the study, with 25 in the AR-group and 25 in the non-AR conventional kinematic alignment group. A 20% attrition rate (10 patients) is expected throughout the study, leaving 20 patients in each study group. The Investigator intend to evaluate only patients who've met the clinical and radiographic indications for TKA for one knee (Killgren Lawrence Grade \> III) and have less than Killgren Lawrence Grade II OA of the contralateral knee. The Investigators intend to use the uninvolved knee as a radiographic comparison to determine ARVIS's post-operative restorative accuracy to the patient's native alignment. Pre- and post-operative radiographs will include standing knee AP, PA, lateral, sunrise, and hip-to-ankle radiographs.
The investigators have chosen to reproduce the patient's native alignment during TKA rather than mechanical alignment given the predominance of recent literature demonstrating superior function and outcome of kinematic based techniques. Intraoperatively, the investigators will use ARVIS to prospectively record bone resection thickness, distal femoral resection angle, femoral component sagittal orientation, femoral component rotation, tibial resection thickness, coronal tibial resection angle, and tibial slope.
The ARVIS is an augmented reality headset with a heads-up display capable of presenting pre-resection hip center and lower extremity alignment. The heads-up display provides real time, intra-operative feedback during bone resections to optimize the component position and lower extremity alignment as compared to the uninvolved contralateral limb. Unlike other methods used to prepare bone cuts during TKA, such as traditional jigs or robotic systems, ARVIS is a self-contained, wearable surgical guidance device controlled by the surgeon, designed to ensure surgeon can focus on their patient while they perform bone cuts on tibia and femur - not a screen across the room.
The procedure of TKA is the same for traditional approach utilizing jigs and ARVIS approach.
ARVIS has received 510(k) clearance from the FDA as of July 2021.
Interventions
- Other Evaluation of Augmented Reality technology in TKA compared to standard TKA
Evaluation of effectiveness of AR system used to perform bone cuts when compared to traditional jigs in primary TKA
Primary outcome measures
- Radiographic Measurements bilateral knees [Time frame: From enrollment until 1 year follow-up visit.]
Secondary outcome measures (4)
- PROMIS-10 Survey [Time frame: frome enrollment until 12 month final study visit]
- Knee Society Score (KSS) [Time frame: From enrollment until final visit at 12 months after surgery]
- Knee Injury and Osteoarthritis outcome Score (KOOS) [Time frame: from enrollment until completion of study at 12 months post surgery]
- Numeric Pain Rating Score (NPRS) [Time frame: From enrollment until final study visit at 12 months post surgery]
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
- 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.
- Patients the Investigator deems not able to follow through with study requirements such as follow-up visits or PROM's.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Other
Study locations
United States · 1 center
- Florida Orthopaedic Institute — Tampa
Identifiers
NCT: NCT06663384 · FORE092024