Total Knee Arthroplasty and Augmented Reality-based Navigation System

June 17, 2024 updated by: Elsan

Does an Augmented Reality-based Navigation System in Total Knee Arthroplasty Allow a Better Alignment of the Lower Limb and Does it Improve Functional Results ? An Equivalence, Monocentric, Prospective and Randomized Study

The purpose of Total Knee Replacement (TKR) is to remove worn cartilage surfaces and replace them with artificial parts of the same shape. TKR can be used in cases of osteoarthritis, inflammatory rheumatism, bone necrosis of the knee or following malformative or traumatic sequelae.

Implant alignment is paramount in TKR and the last years have seen a proliferation of alignment techniques following the introduction of computer and robotic-assisted surgery. Among Computer-assisted surgery, the augmented reality-based navigation system can be an option to improve accuracy in orthopaedic surgery.

The hypothesis of this study is: the use of augmented reality-based navigation system allows a prosthesis alignment and positioning that is at least as good as with the traditional mechanically aligned technique, and therefore improves knee functional results. This study also aims at assessing the cost-effectiveness of this new technology.

Study Overview

Detailed Description

In this randomised study, TKR will be performed either with the traditional mechanically aligned technique or with an augmented reality-based navigation system using Knee+ technology.

Knee+ is a Class Im software medical device (European classification, Directive 93/42/EEC, Annex IX) and obtained CE Mark 0459 in May 2020.

This technology is used in total knee replacement procedures, and offers the orthopedic surgeon intraoperative assistance in positioning the implants with the help of a pair of augmented reality glasses. The cutting planes are oriented with respect to the mechanical axes calculated according to anatomical landmarks acquired with a pointer. The connected glasses calculate precisely the 3D coordinates of the instruments thanks to the analysis of their specific markers (QR-Code), filmed by the integrated camera. The navigation information is displayed in the surgeon's field of vision, who interacts with the application thanks to the glasses' accelerometers.

Study Type

Interventional

Enrollment (Estimated)

88

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Aurillac, France, 15000
        • Centre Médico-Chirurgical de Tronquières

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Gonarthrosis on a varum knee requiring a Total Knee Replacement
  2. Female or male, 18 years of age or older
  3. Affiliation to a social security scheme
  4. Patient has been informed of the study and has signed an informed consent form

Exclusion Criteria:

  1. Osteonecrosis,
  2. Post traumatic osteoarthritis with femoral or tibial callus,
  3. History of tibial or femoral osteotomy,
  4. Valgum knee,
  5. Isolated patellofemoral osteoarthritis,
  6. Significant hip dysplasia or other excessive pelvic deformity,
  7. Patient already equipped with medical devices that may conflict with the instrumentation required for augmented reality navigation,
  8. Pregnant or breastfeeding women,
  9. Patients under legal protection.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: TKR with augmented reality-based navigation system.
This technology offers the orthopedic surgeon intraoperative assistance in positioning the implants with the help of a pair of augmented reality glasses. The cutting planes are oriented with respect to the mechanical axes calculated according to anatomical landmarks acquired with a pointer. The connected glasses calculate precisely the 3D coordinates of the instruments thanks to the analysis of their specific markers (QR-Code), filmed by the integrated camera. The navigation information is displayed in the surgeon's field of vision, who interacts with the application thanks to the glasses' accelerometers.
Surgery
Active Comparator: TKR with traditional mechanically aligned technique.
TKR with traditional mechanically aligned technique will be performed according to local practice and standard guidelines.
As per local practice and standard guidelines.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle
Time Frame: 2 months after surgery
the Hip-Knee-Ankle (HKA) angle is measured on weight bearing pangonogram.
2 months after surgery

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of long-term lower limb alignment between the two procedures
Time Frame: 1 year after surgery
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle on lower limb pangonogram at 1 year after surgery
1 year after surgery
Evaluation of the success of the procedure
Time Frame: 2 months after surgery
The success of the procedure is defined by an HKA angle of 180°
2 months after surgery
Assessment of lower limb alignment variability between the two procedures.
Time Frame: 2 months and1 year after surgery
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle on lower limb pangonogram at 2 months and 1 year after surgery.
2 months and1 year after surgery
Evaluation of radiological measurements between the two procedures
Time Frame: 2 months and1 year after surgery

Evolution of the following radiological parameters at 2 months and 1 year post-surgery:

Femoral valgus Tibial varus Posterior tibial slope Flessum of the femoral implant Patellar tilt

2 months and1 year after surgery
Evaluation of the knee score between the two procedures
Time Frame: 2 months and1 year after surgery
Evolution of the knee score at 2 months and 1 year postoperatively measured by the Knee Society Score (KSS). The KSS is a widely used clinician-assessed outcome score with good published validity data. The clinical part (Knee Score) of the KSS covers pain, range of motion, alignment and stability. The Function Score of the KSS covers patient mobility (walking distance and stairs) and potential walking aids. The KSS scoring scale ranges from 0 to 100 points for each part, with higher scores indicating less severe impairment.
2 months and1 year after surgery
Quality of life assessment between the two procedures
Time Frame: 2 months and1 year after surgery

Change in quality of life at 2 months and 1 year measured by the Short Form-12 (SF-12) questionnaire.

The SF-12 is a standardized self-questionnaire for measuring quality of life.The SF-12 is the shortened version of the SF-36.

The SF-12 is made up of eight subscores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a scale from 0 to 100 on the assumption that each question has the same weight. The lower the score, the greater the handicap. The higher the score, the lower the handicap, i.e. a score of zero equals maximum handicap and a score of 100 equals zero handicap.

2 months and1 year after surgery
Evaluation of knee pain between the two procedures
Time Frame: From day 0 to day 5 ; Once a week during 1 month ; at 2 months ; at 3 months and 1 year after surgery

Evolution of pain every day between D0 (postoperative) and D5, then once a week during the first month, then at 2 months, 3 months and at 1 year postoperative measured by a visual analog scale (VAS).

The visual analog scale (VAS) for pain is a pain self-assessment tool. The patient defines his pain on a line 10cm long. The distance (in millimeters) from the left extremity defines the pain. The value zero corresponds to the lower limit defining the absence of pain and 100 to the upper limit corresponding to "the worst pain imaginable".

From day 0 to day 5 ; Once a week during 1 month ; at 2 months ; at 3 months and 1 year after surgery
Evaluation of the hemoglobin level between the two procedures
Time Frame: From day 1 to day 3 after surgery
Evolution of the hemoglobin level at D1 and D3
From day 1 to day 3 after surgery
Evaluation of the Average Length of Stay between the two procedures
Time Frame: From the day of surgery at the time of hospital discharge up to 1 day
The Average Length of Stay will be evaluated in days from the hospital's entry and exit records.
From the day of surgery at the time of hospital discharge up to 1 day
Evaluation of the postoperative complications rate between the two procedures
Time Frame: During 1 year post-operative

Occurrence of a thromboembolic complication (yes/no) during the 1-year post-operative follow-up.

Occurrence of a surgical site infection (yes/no) during the 1-year post-operative follow-up.

Occurrence of wound healing problems (yes/no) during the 1-year post-operative follow-up

During 1 year post-operative
Evaluation of the Quality-Adjusted Life Years (QALY) between the two procedures
Time Frame: At 1 year
EQ-5D questionnaire at 1 year and collection of all costs during the first postoperative year.
At 1 year

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Radiographic assessment
Time Frame: At 2 months after surgery
The primary endpoint of this research will be radiographic assessment of the Hip-Knee-Ankle (HKA) angle on weight-bearing lower extremity pangonometry at 2 months after surgery.
At 2 months after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Frédéric Dalat, MD, Centre Médico-Chirurgical de Tronquières

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2024

Primary Completion (Estimated)

November 1, 2024

Study Completion (Estimated)

October 1, 2025

Study Registration Dates

First Submitted

January 18, 2022

First Submitted That Met QC Criteria

January 31, 2022

First Posted (Actual)

February 10, 2022

Study Record Updates

Last Update Posted (Actual)

June 18, 2024

Last Update Submitted That Met QC Criteria

June 17, 2024

Last Verified

June 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • TKA and augmented reality
  • 2021-A02549-32 (Other Identifier: ANSM)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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