Kinematics of Contemporary Knee Arthroplasty
Primary Purpose
Knee Osteoarthritis
Status
Active
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Zimmer Biomet NexGen CR
Medacta International GMK Sphere
Sponsored by
About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Total Knee Arthroplasty (TKA), Total knee replacement (TKR), Knee kinematics, Dynamic RSA, Fluoroscopy, Fluoroscopic Roentgen Stereophotogrammetric Analysis (FRSA), Medial pivot, Medially stabilized
Eligibility Criteria
Inclusion Criteria:
1. Patients with knee osteoarthritis
Exclusion Criteria:
- Preoperative severe deformity (Femoro-tibial angle < 175°or > 190° measured on a full-length leg image at weight bearing)
- Preoperative flexion contracture more than 15°
- Preoperative limited range of motion under anesthetics (less than 110°)
- Less than 50 or more than 75 years of age at the time of surgery
- Use of walking aids because of other musculoskeletal and neuromuscular problems
- Preoperative diagnosis other than osteoarthritis and avascular necrosis (e.g. rheumatoid arthritis, tumors)
- Revision arthroplasty
- Obesity with BMI>35
- Impaired collateral ligaments
- Postoperative KOOS score less than 80
- Malposition of femoral and tibial implants (Internally rotated or more han 10° externally rotated implants will be excluded. The rotation of femoral implant is measured on postoperative CT images in reference to surgical epicondylar line. The rotation of tibial implant is determined according to Berger's measurement)
- Limb surgery within 3 months before the analysis
- Postoperative revision surgery due to deep wound infection
Sites / Locations
- Oslo University Hospital, Ullevål
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Zimmer Biomet NexGen CR
Medacta International GMK Sphere
Arm Description
Patients receive a Zimmer Biomet NexGen Total Knee Replacement
Patients receive a Medacta International, GMK Sphere Total Knee Replacement
Outcomes
Primary Outcome Measures
Knee Kinematics measured though all Degrees of freedom (DOF)
Roentgen Fluoroscopic Stereophotogrammetric Analysis (RFSA). We measure all DOFs (i.e. X-Y-Z rotations and translations in degrees and millimeters respectively)
Secondary Outcome Measures
Knee Society Score (KSS)
Patient Reported Outcome Measure (PROM)
Knee injury and Osteoarthritis Outcome Score (KOOS)
PROM
Forgotten Joint Score 12 (FJS-12)
PROM
Range of motion (ROM)
Clinical measurement using goniometer
Hip-knee-ankle angle (HKA-angle)
The axis of the lower extremity after knee arthroplasty
CT-rotation of implants
Evaluation of tibia implant rotation using Berger's method
Clinical stability
Varus-valgus stability in clinical testing
Full Information
NCT ID
NCT02965690
First Posted
November 14, 2016
Last Updated
December 12, 2021
Sponsor
Oslo University Hospital
Collaborators
Helse More and Romsdal Trust
1. Study Identification
Unique Protocol Identification Number
NCT02965690
Brief Title
Kinematics of Contemporary Knee Arthroplasty
Official Title
Comparison of in Vivo Kinematics of Different Implants in ACL-sacrificing vs. Medially Stabilized Arthroplasty (Implant Design Study)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 2016 (undefined)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Helse More and Romsdal Trust
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Total joint replacement is an efficacious treatment for osteoarthritis of hips and knees. Both total knee replacement (TKR) and total hip replacements (THR) have excellent implant survivorship. However, patient satisfaction is lower in TKR than THR. A possible cause of the discrepancy is the unnatural knee kinematics after TKR. Various implant designs have been developed to solve the problem. However, most of the designs are based on experimental data and not on in vivo kinematics. In this study, we will analyze the in vivo kinematics of the Global Medacta Knee Sphere (GMK Sphere) implant and compare it with a well documented design and implant (NexGen Cruciate Retaining (CR), Zimmer Biomet). We assume our study will contribute to the development of more satisfying knee implants.
Detailed Description
Worldwide the number of patients requiring treatment for osteoarthritis is increasing due to increasing obesity, an ageing population and a high demanding younger population. Learmonth describes hip arthroplasty as the "operation of the century" because patients are highly satisfied with pain relief and function after the procedure. Knee arthroplasties have in recent years also shown promising results and have surpassed hip arthroplasty in frequency in western countries. However, patient satisfaction is not as high. Reported problems are insufficient function and persistent pain. On the other hand, knee arthroplasties are increasingly implanted in younger and more active patients who require high function and quality of life. Improvement of results after knee arthroplasty is therefore an urgent issue in the field of orthopaedic research.
Knee kinematics and implant designs:
A possible cause of lower function of replaced knees is the unnatural postoperative knee kinematics. The kinematics of replaced knees are closely related to their function. Studies show that replaced knees with excellent flexion angles have kinematic similarities to normal knees and malalignments of implants can cause postoperative pain.
Compared to the hip joint which is a simple ball-and-socket joint, the kinematics of knee is more complex. Native knee kinematics are a combination of a rolling and gliding motion of the femoral condyles and rotation of the tibia, where roll back of the lateral femoral condyle is larger than medially. Roll back is important for high degrees of flexion. Native knee kinematics are not fully understood, but the anterior cruciate ligament (ACL) seems to be an integral part, as knees without a functioning ACL show decreased roll back. Based on the kinematics of the normal knee joint, various attempts have been made on the design of knee implants to reconstruct normal kinematics after replacement surgery, but in knee osteoarthritis the ACL and posterior cruciate ligament (PCL) is often deficient as they are damaged by inflammation. Therefore, there are three concepts regarding the retaining of these ligaments in knee replacement surgery. 1: Sacrifice both the ACL and PCL, 2: Retain the PCL (cruciate retaining (CR) design), 3: Retain both the ACL and PCL (bicruciate-reataining design).
The function of the cruciate ligaments can be mimicked by different designs of the tibial insert. The CR design has been widely used in the northern countries, especially the Zimmer Biometri NexGen CR implant in Norway. There are migration data for the NexGen implant with high precision measurements available in the literature. However, the NexGen CR implant does not retain the ACL and does not mimic natural knee kinematics.
The tibial insert of the medially stabilized implant design (Medacta International, GMK Sphere) has a constrained medial "ball in socket" joint and at the same time allows lateral anterioposterior movement (roll back). This new design was developed by a group of dedicated researchers. The design intention is to resemble the native kinematics of the knee by mimicing the function of the cruciate ligaments and at the same time allow for lateral anterioposterior movement (rollback). Theoretically, knee implant designs, which retain the function of cruciate ligaments are predicted to have the closest kinematics to normal knees compared to other designs and to have the potential to achieve the highest patient satisfaction.
Analytical Method:
Radiostereometric Analysis (RSA) has been used in orthopedic research fields since 1970s. The original application of this method was for the evaluation of implant migration (i.e. fixation) and polyethylene wear of artificial joints using static X-ray pictures. When combining RSA with fluoroscopy, we get Fluoroscopic Roentgen Stereophotogrammetric Analysis (FRSA), a method with high accuracy and precision. Few implants have been analysed kinematically in vivo. We plan to investigate the knees during in vivo motion and weight-bearing using FRSA.
Purpose of the study:
The aim of this study is to analyse the in vivo kinematics of a medially stabilized knee arthroplasty implant (GMK Sphere) and to compare it with a well known design (Nexgen CR, Zimmer Biomet) by using FRSA.
By using flat panel fluoroscopy, we will document and compare the kinematics of the two implants in all 6 degrees of freedom (DOF).
26 patients will be randomized into two groups, one will receive the NexGen CR prosthesis, the other group the GMK Sphere.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Total Knee Arthroplasty (TKA), Total knee replacement (TKR), Knee kinematics, Dynamic RSA, Fluoroscopy, Fluoroscopic Roentgen Stereophotogrammetric Analysis (FRSA), Medial pivot, Medially stabilized
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective, parallel-group, non-blind, randomized clinical study
Masking
None (Open Label)
Masking Description
Non-blind
Allocation
Randomized
Enrollment
26 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Zimmer Biomet NexGen CR
Arm Type
Active Comparator
Arm Description
Patients receive a Zimmer Biomet NexGen Total Knee Replacement
Arm Title
Medacta International GMK Sphere
Arm Type
Active Comparator
Arm Description
Patients receive a Medacta International, GMK Sphere Total Knee Replacement
Intervention Type
Procedure
Intervention Name(s)
Zimmer Biomet NexGen CR
Intervention Description
Total Knee Replacement
Intervention Type
Procedure
Intervention Name(s)
Medacta International GMK Sphere
Intervention Description
Total Knee Replacement
Primary Outcome Measure Information:
Title
Knee Kinematics measured though all Degrees of freedom (DOF)
Description
Roentgen Fluoroscopic Stereophotogrammetric Analysis (RFSA). We measure all DOFs (i.e. X-Y-Z rotations and translations in degrees and millimeters respectively)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Knee Society Score (KSS)
Description
Patient Reported Outcome Measure (PROM)
Time Frame
1 year
Title
Knee injury and Osteoarthritis Outcome Score (KOOS)
Description
PROM
Time Frame
1 year
Title
Forgotten Joint Score 12 (FJS-12)
Description
PROM
Time Frame
1 year
Title
Range of motion (ROM)
Description
Clinical measurement using goniometer
Time Frame
1 year
Title
Hip-knee-ankle angle (HKA-angle)
Description
The axis of the lower extremity after knee arthroplasty
Time Frame
1 year
Title
CT-rotation of implants
Description
Evaluation of tibia implant rotation using Berger's method
Time Frame
1 year
Title
Clinical stability
Description
Varus-valgus stability in clinical testing
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1. Patients with knee osteoarthritis
Exclusion Criteria:
Preoperative severe deformity (Femoro-tibial angle < 175°or > 190° measured on a full-length leg image at weight bearing)
Preoperative flexion contracture more than 15°
Preoperative limited range of motion under anesthetics (less than 110°)
Less than 50 or more than 75 years of age at the time of surgery
Use of walking aids because of other musculoskeletal and neuromuscular problems
Preoperative diagnosis other than osteoarthritis and avascular necrosis (e.g. rheumatoid arthritis, tumors)
Revision arthroplasty
Obesity with BMI>35
Impaired collateral ligaments
Postoperative KOOS score less than 80
Malposition of femoral and tibial implants (Internally rotated or more han 10° externally rotated implants will be excluded. The rotation of femoral implant is measured on postoperative CT images in reference to surgical epicondylar line. The rotation of tibial implant is determined according to Berger's measurement)
Limb surgery within 3 months before the analysis
Postoperative revision surgery due to deep wound infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Frank-David Oehrn, MD
Organizational Affiliation
CIRRO and Kristiansund Hospital, Helse More and Romsdal Trust
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stephan Maximillian Røhrl, PhD
Organizational Affiliation
CIRRO and Oslo University Hospital, Ullevål
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Lars Harald William Engseth, MD
Organizational Affiliation
CIRRO and Oslo University Hospital, Ullevål
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oslo University Hospital, Ullevål
City
Oslo
ZIP/Postal Code
0470
Country
Norway
12. IPD Sharing Statement
Plan to Share IPD
No
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Kinematics of Contemporary Knee Arthroplasty
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