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Total Knee Arthroplasty and Augmented Reality-based Navigation System

Primary Purpose

Gonarthrosis

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
TKR with augmented reality-based navigation system
TKR with traditional mechanically aligned technique
Sponsored by
Elsan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gonarthrosis focused on measuring TKR: total knee replacement

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Centre Médico-Chirurgical de Tronquières

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TKR with augmented reality-based navigation system.

TKR with traditional mechanically aligned technique.

Arm Description

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.

TKR with traditional mechanically aligned technique will be performed according to local practice and standard guidelines.

Outcomes

Primary Outcome Measures

Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle
the Hip-Knee-Ankle (HKA) angle is measured on weight bearing pangonogram.

Secondary Outcome Measures

Evaluation of long-term lower limb alignment between the two procedures
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle on lower limb pangonogram at 1 year after surgery
Evaluation of the success of the procedure
The success of the procedure is defined by an HKA angle of 180°
Assessment of lower limb alignment variability between the two procedures.
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle on lower limb pangonogram at 2 months and 1 year after surgery.
Evaluation of radiological measurements between the two procedures
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
Evaluation of the knee score between the two procedures
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.
Quality of life assessment between the two procedures
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.
Evaluation of knee pain between the two procedures
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".
Evaluation of the hemoglobin level between the two procedures
Evolution of the hemoglobin level at D1 and D3
Evaluation of the Average Length of Stay between the two procedures
The Average Length of Stay will be evaluated in days from the hospital's entry and exit records.
Evaluation of the postoperative complications rate between the two procedures
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
Evaluation of the Quality-Adjusted Life Years (QALY) between the two procedures
EQ-5D questionnaire at 1 year and collection of all costs during the first postoperative year.

Full Information

First Posted
January 18, 2022
Last Updated
October 10, 2023
Sponsor
Elsan
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1. Study Identification

Unique Protocol Identification Number
NCT05233930
Brief Title
Total Knee Arthroplasty and Augmented Reality-based Navigation System
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 2023 (Anticipated)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
May 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Elsan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gonarthrosis
Keywords
TKR: total knee replacement

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomised, double-arms, parallel, open-label study.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
88 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TKR with augmented reality-based navigation system.
Arm Type
Experimental
Arm Description
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.
Arm Title
TKR with traditional mechanically aligned technique.
Arm Type
Active Comparator
Arm Description
TKR with traditional mechanically aligned technique will be performed according to local practice and standard guidelines.
Intervention Type
Procedure
Intervention Name(s)
TKR with augmented reality-based navigation system
Intervention Description
Surgery
Intervention Type
Procedure
Intervention Name(s)
TKR with traditional mechanically aligned technique
Intervention Description
As per local practice and standard guidelines.
Primary Outcome Measure Information:
Title
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle
Description
the Hip-Knee-Ankle (HKA) angle is measured on weight bearing pangonogram.
Time Frame
2 months after surgery
Secondary Outcome Measure Information:
Title
Evaluation of long-term lower limb alignment between the two procedures
Description
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle on lower limb pangonogram at 1 year after surgery
Time Frame
1 year after surgery
Title
Evaluation of the success of the procedure
Description
The success of the procedure is defined by an HKA angle of 180°
Time Frame
2 months after surgery
Title
Assessment of lower limb alignment variability between the two procedures.
Description
Radiographic evaluation of the Hip-Knee-Ankle (HKA) angle on lower limb pangonogram at 2 months and 1 year after surgery.
Time Frame
2 months and1 year after surgery
Title
Evaluation of radiological measurements between the two procedures
Description
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
Time Frame
2 months and1 year after surgery
Title
Evaluation of the knee score between the two procedures
Description
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.
Time Frame
2 months and1 year after surgery
Title
Quality of life assessment between the two procedures
Description
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.
Time Frame
2 months and1 year after surgery
Title
Evaluation of knee pain between the two procedures
Description
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".
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
Title
Evaluation of the hemoglobin level between the two procedures
Description
Evolution of the hemoglobin level at D1 and D3
Time Frame
From day 1 to day 3 after surgery
Title
Evaluation of the Average Length of Stay between the two procedures
Description
The Average Length of Stay will be evaluated in days from the hospital's entry and exit records.
Time Frame
From the day of surgery at the time of hospital discharge up to 1 day
Title
Evaluation of the postoperative complications rate between the two procedures
Description
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
Time Frame
During 1 year post-operative
Title
Evaluation of the Quality-Adjusted Life Years (QALY) between the two procedures
Description
EQ-5D questionnaire at 1 year and collection of all costs during the first postoperative year.
Time Frame
At 1 year
Other Pre-specified Outcome Measures:
Title
Radiographic assessment
Description
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.
Time Frame
At 2 months after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Gonarthrosis on a varum knee requiring a Total Knee Replacement Female or male, 18 years of age or older Affiliation to a social security scheme Patient has been informed of the study and has signed an informed consent form Exclusion Criteria: Osteonecrosis, Post traumatic osteoarthritis with femoral or tibial callus, History of tibial or femoral osteotomy, Valgum knee, Isolated patellofemoral osteoarthritis, Significant hip dysplasia or other excessive pelvic deformity, Patient already equipped with medical devices that may conflict with the instrumentation required for augmented reality navigation, Pregnant or breastfeeding women, Patients under legal protection.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Frédéric Dalat, MD
Phone
04 71 45 42 54
Ext
+33
Email
fred.dalat@hotmail.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frédéric Dalat, MD
Organizational Affiliation
Centre Médico-Chirurgical de Tronquières
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Médico-Chirurgical de Tronquières
City
Aurillac
ZIP/Postal Code
15000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
30611520
Citation
Panjwani TR, Mullaji A, Doshi K, Thakur H. Comparison of Functional Outcomes of Computer-Assisted vs Conventional Total Knee Arthroplasty: A Systematic Review and Meta-Analysis of High-Quality, Prospective Studies. J Arthroplasty. 2019 Mar;34(3):586-593. doi: 10.1016/j.arth.2018.11.028. Epub 2018 Dec 2.
Results Reference
background
PubMed Identifier
22130355
Citation
Cheng T, Pan XY, Mao X, Zhang GY, Zhang XL. Little clinical advantage of computer-assisted navigation over conventional instrumentation in primary total knee arthroplasty at early follow-up. Knee. 2012 Aug;19(4):237-45. doi: 10.1016/j.knee.2011.10.001. Epub 2011 Nov 29.
Results Reference
background
Links:
URL
https://pubmed.ncbi.nlm.nih.gov/30611520/
Description
Computer-assisted navigation system (CAS) in total knee arthroplasty (TKA) has been shown to improve mechanical alignment and prosthesis positioning as compared to conventional TKA.
URL
https://pubmed.ncbi.nlm.nih.gov/22130355/
Description
Even though computer-assisted navigation systems have been shown to improve the accuracy of implantation of components into the femur and tibia, long-term results are lacking

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Total Knee Arthroplasty and Augmented Reality-based Navigation System

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