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NCT Number: NCT06787417

Kinematic and Mechanical Alignment Randomized Trial

Knee replacement surgery is the second most common surgery in Canada. People who have very painful knee arthritis usually receive a knee replacement where the surgeon aims to make everyone's knee as straight as possible (called mechanical alignment). Mechanical alignment focuses on making the implant last as long as possible. However, everybody's knee shape is different and we think that it is important to take individual differences into account. A newer technique that is more personalized is called restricted kinematic alignment. This technique customizes the placement of the new knee to reproduce each patient's unique knee shape, which may not be perfectly straight. We think this newer technique may feel more natural, be more stable, and lead to better knee function. Restricted kinematic alignment might last as long or longer than mechanical alignment, but the research that has been conducted to date is not clear. We are conducting this study to help surgeons better understand which technique is better. One of the reasons the existing research is not clear is because new developments in robotic technology now allow surgeons to place knee implants very precisely, which was not done in most previous research. In this study everyone will receive a robot-assisted knee surgery so we can be sure the implants are placed as precisely as possible.

The purpose of this trial is to determine whether there are differences in patient outcomes using restricted kinematic alignment rather than the traditionally used mechanical alignment for total knee replacements.

Participants who are having total knee replacements will be randomized to receive either a robot-assisted total knee replacement using mechanical alignment, or a robot-assisted total knee replacement using restricted kinematic alignment . We will ask participants to walk in a markerless motion capture system which will measure walking characteristics at pre-op, 6 months postop and 12 months postop. Participants will also complete a series of standardized questionnaires at preop and 6 months, 12 months, and 24 month postop.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

St. Joseph's Healthcare

Hamilton, Ontario, L8N 4A6, Canada

Location status: Recruiting

Location contact

Anthony Adili, MD, P.Eng, FRCSC

PRINCIPAL_INVESTIGATOR

Kim Madden, PhD

CONTACT

[email protected]

289-237-7380

About this study

Total Knee Arthroplasty (TKA) is recognized as a highly effective procedure for alleviating pain and restoring function in patients with knee arthritis. Despite its high success rate, approximately 20% of patients remain dissatisfied with the outcomes, primarily due to loss of functional outcomes, persistent pain, and reduced knee range of motion. This has sparked a debate on the optimal surgical alignment technique in TKA-whether mechanical alignment (MA), or personalized alignment philosophies such as kinematic alignment (KA) or restricted kinematic alignment (rKA) provides superior patient outcomes.

MA traditionally targets a neutral 180-degree hip-knee-ankle (HKA) axis, as it was taught traditionally that this approach focuses on the longevity and stability of the implant. However, this one-size-fits-all philosophy overlooks individual anatomical differences. Personalized alignments such as KA customize the placement of prosthetic components to replicate each patient's unique knee geometry and ligament tensions. Personalized alignment philosophies aim to achieve a more natural knee motion, which may enhance patient satisfaction. The precision provided by robotic-assisted surgery has increasingly facilitated the implementation of personalized alignment philosophies in TKA. Recent evidence suggests that while MA and KA yield comparable outcomes in terms of knee functionality and motion, KA may improve satisfaction and the natural feel of the knee in certain groups, particularly those without severe preoperative deformities. There is also the emerging approach of restricted kinematic alignment (rKA) which aims to provide a compromise by aligning the prosthesis within safe anatomical limits, thus avoiding the extremes of anatomical variation. This approach tailors the surgery more closely to the individual's anatomy without the risks associated with the broader variances permitted in pure KA. Hypothetically, KA and rKA techniques should more closely replicate natural knee biomechanics and improve waking gait. There are advantages and disadvantages to these alignment philosophies which should be addressed with high-quality research. While there have been several previous randomized trials on MA vs KA and its variations, the evidence is still unclear with meta-analyses having conflicting findings.

Patients will be randomly assigned to either mechanical alignment or restricted kinematic alignment. All participants will receive robot-assisted TKA using the Stryker Mako surgical robot and Stryker implants. Perioperative care, postoperative pain medications, and rehabilitation will be standardized according to local standard care.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult aged 18 years or older
  • Knee osteoarthritis requiring total knee arthroplasty
  • Provide informed consent

Exclusion criteria

  • Inability to provide informed consent (e.g. cognitive disability, language barrier)
  • Revision knee surgery
  • Simultaneous bilateral knee surgery
  • Recent lower extremity surgery or trauma interfering with gait assessment
  • A CT scan cannot be obtained prior to surgery
  • Inability or unwillingness to comply with the study protocol

Treatment and study plan

Restricted Kinematically-aligned Arthroplasty

Procedure

Robot Assisted with Restricted Kinematically-Aligned TKA.

Mechanically-Aligned Arthroplasty

Procedure

Robot Assisted with Mechanically Aligned TKA.

Primary outcomes

  1. Gait Biomechanics

    Time frame: 12 months

    The primary outcome will be joint angles and walking characteristics (speed, step length, number of steps, consistency between sides) collected using an in-clinic markerless motion capture system. The system uses 10 synchronized optical cameras (60 Hz, Sony RXOII) placed strategically along the clinic hallways to maximize the viewing volume to capture patient movement characteristics. Advanced AI-driven software (Theia Markerless) is used to predict limb segment poses dynamically as the person moves through the space, and, combined with biomechanical modelling algorithms (Visual3D, C-Motion) can be used to accurately represent patient lower extremity 3D joint angles and other kinematic stride characteristics.

Secondary outcomes

  1. Knee function

    Time frame: 24 months

    We will measure knee function using the Forgotten Joint Score (FJS-Knee). The FJS-Knee is a well validated and well-used 12 item questionnaire specifically used to measure function in elation to how natural a knee feels after total knee replacement surgery

  2. Chronic post-surgical pain (CPSP)

    Time frame: 24 months

    We will use a modified version of the International Association for the Study of Pain's (IASP) definition of CPSP, to include a minimum threshold of pain severity: 1) Pain that developed after surgery; 2) Pain that lasts at least 3 months; 3) Other causes of pain have been excluded; 4) Pain caused by other conditions have been excluded; 5) Pain intensity at least 3/10 on a numeric rating score.

  3. Quality of life

    Time frame: 24 months

    We will use the Euro-Qol 5 Dimensions-5L (EQ-5D-5L) questionnaire to assess health-related quality of life (HRQoL). The EQ-5D-5L is a well-validated and well-used quality of life instrument that can assess health utilities

  4. Return to Function

    Time frame: 24 months

    We will use the Return To Function (RTF) questionnaire developed by Busse et al. at McMaster University. The RTF questionnaire is a 5 item questionnaire that has been used previously in orthopaedic trials to determine when a trial participant returns to work, leisure, and activities around the home after an injury or surgery

Other outcomes

  1. Safety

    Time frame: 24 months

    We will collect all reoperations, serious adverse events (SAEs) and surgery-related non-serious AEs throughout the trial for safety monitoring purposes

Study contacts

Contact information is provided by the study sponsor or research team.

Kim Madden, PhD

CONTACT

[email protected]

289-237-7380

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Collaborators

  • Canadian Orthopaedic Foundation (funding)
  • Research Institute of St. Joseph's Hamilton

Registry information

Official study title

Kinematic and Mechanical Alignment Randomized Trial (KMART): A Technology-Focused Randomized Controlled Trial

Acronym: KMART

Important dates

Study start
2025
Primary completion
2028
Study completion
2029
First posted
Jan 22, 2025
Registry last updated
May 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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