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Personal SatisfactionNCT02256904

RSA and Clinical Comparison of Anatomical and Mechanical Alignment in Total Knee Replacement

A study testing Anatomical TKA and Mechanical TKA in people with Personal Satisfaction and Genu Varum, run by Maisonneuve-Rosemont Hospital at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Current practice in orthopedics is to recommend TKA implantation with the femoral and tibial components perpendicular to their mechanical axis. Therefore, current surgical technique does not replicate natural knee anatomy and biomechanics. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Personal Satisfaction, Genu Varum
What is being tested?
Anatomical TKA and Mechanical TKA
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
134 participants
Where
1 siteCanada
Study dates
13 Apr 2015to Jan 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patient qualifies for primary TKA
  • Patient understands the study conditions
  • Patient is capable of giving informed consent

Who cannot join

  • Other joint damage of the lower limbs
  • Extra-articular knee deformation of the lower limb
  • Hip arthroplasty on the surgical side
  • Contraindication to CT-scan
  • Acute or chronic infection of the lower limb
  • Progressive local or systemic infection
Show all 14Show fewer
  • Alcohol or drug abuse
  • Psychiatric illness/mental disorder
  • Pregnancy
  • Less than 18 years of age
  • Known allergy to the implant materials
  • Muscular loss, neuromuscular disease or vascular deficiency of the affected limb making the operation unjustifiable
  • Any neuromuscular disorder
  • Severe instability secondary to advanced destruction of osteochondral structures or loss of integrity of the lateral ligament

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Hopital Maisonneuve Rosemont

    Montreal, Quebec, H1T 2M4

Other trials in Canada

About this study

Official title: Biomechanical and Radiostereometric Analysis of the GMK Sphere Primary Total Knee Replacement. A Randomized, Double Blind Comparison of Anatomical Versus Mechanical Alignment in Total Knee Replacement.

Current practice in orthopedics is to recommend TKA implantation with the femoral and tibial components perpendicular to their mechanical axis. Therefore, current surgical technique does not replicate natural knee anatomy and biomechanics. An alternative alignment method that attempts to replicate the kinematics of the knee is " kinematic alignment ". The principle behind kinematic alignment is placement of the TKA components so that the orthogonal 3-D orientation of the 3 axes that describe normal knee kinematics is restored to that of the prearthritic knee. Theoretical benefits of kinematic alignment include less ligamentous release to balance the knee intra-operatively, more rapid recovery, better range of motion (ROM), less post-operative pain, better knee biomechanics, and improved patient satisfaction. However, a major concern is that there are no mid- or long-term data on implant survivorship (absence of loosening) in TKA based on "anatomical" implantation. The investigators propose to compare the clinical results of TKA implanted with mechanical alignment (standard practice) to kinematic alignment, in a double-blind, randomized trial.

Read the detailed description

Problem to be addressed Knee osteoarthritis is a degenerative joint disease that is very prevalent in the general population and can cause significant functional impairment. Total knee arthroplasty (TKA) is the definitive treatment of choice, but rarely accomplishes complete restoration of natural knee biomechanics. Various factors may influence post-operative function: pre-operative state of the knee, patient age, implant position, and design. The natural lower limb anatomy presents a femoral joint surface that is slightly valgus according to its mechanical axis (1-5 degrees) and a tibial joint surface that is slightly varus (1-4 degrees). This combination results in an oblique joint line orientation (1-3 degrees) and a mechanical axis passing near the centre of the knee joint (line between the centre of the femoral head and the centre of the ankle). Natural lower limb alignment helps balancing load between the internal and external knee compartments at heel strike. Current practice in orthopedics is to recommend TKA implantation with the femoral and tibial components perpendicular to their mechanical axis (0 degrees). In addition, in order to maintain ligament balance (a rectangular space) in flexion, external rotation of the femoral implant is suggested (2-5 degrees according to posterior femoral condyle surfaces). Therefore, current surgical technique does not replicate natural knee anatomy and biomechanics. An alternative alignment method that attempts to replicate the kinematics of the knee is " kinematic alignment ". The principle behind kinematic alignment is placement of the TKA components so that the orthogonal 3-D orientation of the 3 axes that describe normal knee kinematics is restored to that of the prearthritic knee. Theoretical benefits of kinematic alignment include less ligamentous release to balance the knee intra-operatively, more rapid recovery, better range of motion (ROM), less post-operative pain, better knee biomechanics, and improved patient satisfaction. However, a major concern is that there are no mid- or long-term data on implant survivorship (absence of loosening) in TKA based on "anatomical" implantation. Because the anatomical alignment differs from the classic mechanical alignment, some authors raised concerns regarding mid-term implant stability with the anatomical implantation technique.

We propose to compare the clinical results of TKA implanted with mechanical alignment (standard practice) to kinematic alignment, in a double-blind, randomized trial. To standardize surgical technique and minimize potential bias, both procedures will be undertaken with personalized instruments built by Medacta, based on each patient's CT-scan.

There are 2 primary objectives of this research. First, implant stability with respect to bone will be measured over time by RSA, and long-term survivorship will be estimated. Second, we will determine if anatomical implantation provides clinical advantages, with respect to knee kinematic analysis, functional performance tests and validated self-reported questionnaires on pain, function and stiffness.

Radiostereometric analysis (RSA) RSA, first developed in Lund, Sweden, is a radiographic technique for accurately assessing implant position relative to host bone. RSA is the gold standard for measuring implant stability in the short-term and predicting implant survivorship in the long-term. It has been implemented for several decades and its safety is well documented. RSA is 10 times more accurate than conventional radiography in analyzing implant migration patterns. Patterns of micromigration exhibited by various prostheses and fixation techniques within the first post-operative year has been shown to predict long-term component fixation to bone.

Knee biomechanical evaluation Estimating the therapeutic efficacy of knee TKA is subjective in current clinical practice because methods of functional biomechanics assessment are complex and difficult to apply. It was suggested that gait measurements should be monitored after surgery for patients with knee osteoarthritis (OA) to evaluate treatment outcome and recovery. KneeKGTM (Emovi Inc., Laval, Quebec, Canada), a simple and minimally-invasive method of measuring 3D knee kinematics, has been developed and is now available commercially. In this system, motion sensors are quasi-rigidly attached to the leg with a non-invasive ancillary system, which reduces errors in skin movement in relation to bone. This measurement tool has been validated by satisfactory assessment of its accuracy and the reproducibility of femoro-tibial 3D kinematics during gait.

Principal research questions

  • Compare the migration between anatomically- and mechanically-aligned implants at 2 years and predict the long-term survivorship of total knee prostheses inserted with these two techniques.
  • Compare the clinical results of anatomical and mechanical total knee alignment with self reported pain, function and stiffness questionnaire scores.
  • Compare knee kinematics between the 2 groups and identify biomechanical markers that explain subjective differences (if found with clinical scores).
  • Compare kinematics measured with the 2 techniques to those of asymptomatic knees.
  • Determine if anatomical alignment offers some technical benefits (reduced intra-operative ligament balance and ligaments releases) compared to a mechanical alignment technique.
  • Compare post-operative rehabilitation in both groups (flexion, extension, straight leg raising, walking without assistance, etc.).

Hypothesis TKA implanted with with anatomical alignment will provide better clinical outcomes and knee kinematics closer to normal than TKA implanted with a mechanical alignment technique, Implant longevity will show similar micro migration patterns between the two groups as measured by RSA up to 2 years after implantation thereby predicting that long-term implant survivorship will be similar in both groups.

Why is this trial needed now? Current technological advances in knee arthroplasty surgery have allowed surgeons to implant TKA with considerable accuracy. We however are not sure if the position we are placing the knee in is the "correct" position for most patients. It is thought that the relatively high percentage of patients that are not completely satisfied with the outcome of their knee replacement may have the implants in a suboptimal position for that individual patient. The traditional mechanical alignment may not be the optimal position for these patients. The anatomical alignment technique may reduce the percentage of dissatisfied patients. Implant companies with this technology are currently marketing this to surgeons and patients without clinical data to support this claim. There is also the possibility that placing an artificial knee joint in an anatomic position may impart a negative impact on longevity of the implant, thus increasing early revision rates and the significant health costs associated with this. Thus it becomes mandatory to evaluate this new technology before its widespread adoption in clinical practice to determine the real benefits or disadvantages of changing from a successful clinical practice (mechanical alignment) used over the last 40 years.

Trial results This proposed clinical trial will have a direct impact on patient care if it demonstrates that anatomical alignment TKA provides better clinical results than mechanical alignment TKA and similar migration patterns measured by RSA. Then the use of anatomic alignment may become the gold standard for TKA procedures. Lacking accurate investigation and surgical tools, anatomical alignment was abandoned in the early TKA era. Mechanical alignment was selected to minimize errors and secondary failures. With novel technologies (personalized instruments built on MRI), anatomical alignment might be the best way to replicate knee biomechanics and improve patient outcomes after TKA. The proposed study will allow us to establish the real value of anatomical alignment and its safety.

Being tested
Anatomical TKA, Mechanical TKA
Keywords
Alignment, Kinematic, knee, satisfaction, function, survivorship
Medical subject headings
Personal Satisfaction, Genu Varum

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Anatomical TKAProcedure or surgery

    Personalized Medacta plastic cutting blocks will be manufactured according to patient Ct-scan.The anatomical cutting blocks will be design to resurface the femoral and tibial bones to restore each patient's pre-arthritic anatomy within specific margins: maximum of 5 degrees valgus/varus tibial or femoral cut and overall lower limb alignment within +/-3 degrees of varus/valgus). GMK sphere TKA will be implanted using the manufactured cutting blocks.

  • Mechanical TKAProcedure or surgery

    Personalized Medacta plastic cutting blocks will be manufactured according to patient Ct-scan. In the mechanical group, femoral and tibial cutting blocks will be designed for a 0-degree angle according to the mechanical axis. Femoral rotation will be aligned with the femoral trans-epicondylar axis. Tibial rotation will follow femoral rotation. GMK sphere TKA will be implanted using the manufactured cutting blocks.

Study groups in NCT02256904
Study groupRoleWhat they receive
AnatomicalExperimental67 subjects will be randomized to receive an Anatomical TKA with the My knee instruments and a GMK sphere device.
Receives: Procedure: Anatomical TKA
MechanicalActive comparator67 subjects will be randomized to receive a Mechanical TKA with the My knee instruments and the GMK sphere device.
Receives: Procedure: Mechanical TKA

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Component migration measured with Radiostereophotometry

    In the first 40 cases (20 in each group), we will compare the migration with a RSA system between anatomically- and mechanically-aligned implants at 2 years and predict the long-term survivorship of total knee prostheses inserted with these two techniques.

    Measured: 2 years

Secondary outcomes (4)
  1. Clinical scores

    In all randomized subject, we will compare the clinical results of anatomical and mechanical total knee alignment with self reported pain, function and stiffness questionnaire scores. Validated clinical scores will be used: WOMAC, KOOS and SF-12

    Measured: 2 years

  2. Knee kinematics measured with the Knee KG (Emovi inc.)

    In all randomized cases, we will compare post operative knee kinematics with the Knee KG system (Emovi inc) between the 2 groups and identify biomechanical markers that explain subjective differences (if found with clinical scores).

    Measured: 2 years

  3. Technical benefits

    In all randomized cases, we will determine if anatomical alignment offers some technical benefits (reduced intra-operative ligament balance and ligaments releases) compared to a mechanical alignment technique.

    Measured: 1 month

  4. Rehabilitation

    In all cases, we will compare post-operative rehabilitation in both groups (flexion, extension, straight leg raising, walking without assistance, etc.).

    Measured: 1 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2014 (estimated)
  2. Study start13 Apr 2015
  3. Primary completion15 Oct 2019
  4. Study completionJan 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
134 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02256904
Sponsor's protocol ID
HMR 01
Status last verified
Mar 2023
First submitted
30 Sep 2014
Last updated
17 Mar 2023
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Anatomical TKA and Mechanical TKA in people with Personal Satisfaction and Genu Varum, run by Maisonneuve-Rosemont Hospital at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 17 Mar 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Component migration measured with Radiostereophotometry (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Mar 2023.

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