Function, Pain, and Alignment Following Knee Replacement for the Treatment of Osteoarthritis

Sponsor
North York General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05490186
Collaborator
(none)
300
1
3
26.5
11.3

Study Details

Study Description

Brief Summary

There are many factors that can influence patient satisfaction and patient related outcomes following total knee replacement including the surgical alignment of the joint components. Historically, total knee replacements have been performed with an aim aiming to achieve neutral alignment or a mechanical weight axis in the lower extremity . However, only 0.1 % of the population have a pre-surgical anatomical neutral alignment, and therefore the constitutional anatomy of the patient is neglected. There is a growing trend to return patients back their anatomical constitutional alignment after a knee replacement, referred to as Kinematic Alignment using robotics. The aim of this randomized controlled trial is to examine how mechanical alignment and kinematic alignment impacts function, pain, mood and fatigue following TKR for the treatment of osteoarthritis. Outcomes will be measured at 6 week, 6 months, 1 year and 2 years after surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Total Knee Replacement
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Function, Pain, and Alignment Following Knee Replacement for the Treatment of Osteoarthritis
Actual Study Start Date :
Nov 16, 2021
Anticipated Primary Completion Date :
Jan 31, 2023
Anticipated Study Completion Date :
Jan 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Manual Adjusted Mechanical Alignment

Usual care: Midline incision, no tourniquet, medial Parapatellar arthrotomy, resect anterior osteophytes Distal femoral cut with 3-5 degrees of valgus from the anatomical axis (Based on the angle measurement on the 4 foot standing Xray). Correct for flexion contracture. Measure the femoral size with the anterior referencing guides. Use 3 degrees external rotation to the Posterior condylar axis Perform anterior, posterior and chamfer cuts with the 4 in 1 in appropriate external rotation Extramedullary tibial alignment guide with 3-5 degrees posterior slope, and orthogonal cut to the tibial axis. Resect posterior osteophytes Place trial components and perform appropriate release/balance the gaps Patellar replacement based on surgeon's discretion Cementing the components with tourniquet inflation

Procedure: Total Knee Replacement
Surgical technique for Total knee replacement will be standardized with a MicroPort prosthetic knee joint, patella replacement is optional based on the surgeon's assessment. The participants will receive local anesthetic infiltration by the surgeon, and a similar anesthetic technique with spinal anesthesia using epidural morphine and single shot peripheral nerve blocks. They will receive weight based antibiotics and tranexamic acid. Participants will be randomized to one of three groups. 1)Manual adjusted mechanical knee alignment (usual care) involves the surgeon manually. 2) Robot assisted surgery will include using the ROSA© device from Zimmer©. Robot assisted mechanical alignment aims for neutral alignment of the knee joint. 3) Robot assisted restricted kinematic alignment aims to place the knee joint closer to the participant's anatomical positioning.
Other Names:
  • Manual Adjusted Mechanical Alignment
  • Robotic Assisted Adjusted Mechanical Alignment
  • Robotic Assisted Kinematic Alignment: (Joint line restoration)
  • Experimental: Robotic Assisted Adjusted Mechanical Alignment

    Midline incision, no tourniquet, medial Parapatellar arthrotomy, resect anterior osteophytes Place the femoral pins in the proximal incision and the tibial pins 4 finger breadths under the joint line Map the knee and perform evaluation Assess gaps, adjust the femoral axis to decrease soft tissue release (+/- 2 degrees), correct for flexion contracture Verify and perform distal femoral cut, proximal tibial cut orthogonal (90 Degrees) to the tibial axis Assess and balance extension gap with appropriate releases Remap the posterior condylar axis, assess the flexion space, 3 degrees external rotation to the posterior condylar axis Perform anterior, posterior and chamber cuts with the 4 in 1 (appropriate external rotation), followed by posterior osteophyte resection Place trial components and balance the knee, soft tissue releases (1-2 mm) Patellar replacement based on surgeon's discretion Cementing the components with tourniquet inflation

    Procedure: Total Knee Replacement
    Surgical technique for Total knee replacement will be standardized with a MicroPort prosthetic knee joint, patella replacement is optional based on the surgeon's assessment. The participants will receive local anesthetic infiltration by the surgeon, and a similar anesthetic technique with spinal anesthesia using epidural morphine and single shot peripheral nerve blocks. They will receive weight based antibiotics and tranexamic acid. Participants will be randomized to one of three groups. 1)Manual adjusted mechanical knee alignment (usual care) involves the surgeon manually. 2) Robot assisted surgery will include using the ROSA© device from Zimmer©. Robot assisted mechanical alignment aims for neutral alignment of the knee joint. 3) Robot assisted restricted kinematic alignment aims to place the knee joint closer to the participant's anatomical positioning.
    Other Names:
  • Manual Adjusted Mechanical Alignment
  • Robotic Assisted Adjusted Mechanical Alignment
  • Robotic Assisted Kinematic Alignment: (Joint line restoration)
  • Experimental: Robotic Assisted Kinematic Alignment: (Joint line restoration)

    -- Midline incision, no tourniquet, medial parapatellar arthrotomy, resect anterior osteophytes Place femoral pins in proximal incision, tibial pins 4 finger breadths under joint line Map and evaluate the knee, ROM, varus valgus testing at 0 & 90 degrees flexion Distal femoral cut based on cartilage loss on medial and lateral femoral condyle (9mm total cut/condyle). Perform distal femoral cut, maintain the joint line (femoral axis +/- 5 degrees) Perform proximal tibial cut within +/- 3 degrees, balance the gaps, differential between medial and lateral gaps = 1- 3mm. Assess extension space, resect posterior osteophytes Remap posterior condylar axis, place 4 in 1 at 0 degrees to the post condylar axis (aim = 9mm posterior condylar cuts) Resect posterior osteophytes, place trial components. Adjust cuts to achieve a balanced knee, maintain HKA axis +/- 3 degrees Patellar replacement per surgeon discretion Cement the components with tourniquet inflation

    Procedure: Total Knee Replacement
    Surgical technique for Total knee replacement will be standardized with a MicroPort prosthetic knee joint, patella replacement is optional based on the surgeon's assessment. The participants will receive local anesthetic infiltration by the surgeon, and a similar anesthetic technique with spinal anesthesia using epidural morphine and single shot peripheral nerve blocks. They will receive weight based antibiotics and tranexamic acid. Participants will be randomized to one of three groups. 1)Manual adjusted mechanical knee alignment (usual care) involves the surgeon manually. 2) Robot assisted surgery will include using the ROSA© device from Zimmer©. Robot assisted mechanical alignment aims for neutral alignment of the knee joint. 3) Robot assisted restricted kinematic alignment aims to place the knee joint closer to the participant's anatomical positioning.
    Other Names:
  • Manual Adjusted Mechanical Alignment
  • Robotic Assisted Adjusted Mechanical Alignment
  • Robotic Assisted Kinematic Alignment: (Joint line restoration)
  • Outcome Measures

    Primary Outcome Measures

    1. Function [post-operatively 1 year]

      Oxford knee score

    Secondary Outcome Measures

    1. Quality of Life following knee surgery [post-operatively at 2 years]

      EuroQol 5D index

    2. Quality of Life following knee surgery [post-operatively at 6 weeks]

      EuroQol 5D index

    3. Quality of Life following knee surgery [post-operatively at 6 months]

      EuroQol 5D index

    4. Quality of Life following knee surgery [post-operatively at 1 year]

      EuroQol 5D index

    5. Pain intensity and effectiveness of analgesics [Post-operatively at 6 weeks]

      Brief Pain Inventory-Short Form - Pain Severity Index

    6. Pain intensity and effectiveness of analgesics [Post-operatively at 6 months]

      Brief Pain Inventory-Short Form - Pain Severity Index

    7. Pain intensity and effectiveness of analgesics [Post-operatively at 1 year]

      Brief Pain Inventory-Short Form - Pain Severity Index

    8. Pain intensity and effectiveness of analgesics [Post-operatively at 2 years]

      Brief Pain Inventory-Short Form - Pain Severity Index

    9. Satisfaction with knee surgery [Post-operatively at 6 weeks, 6 months, 1 year and 2 years]

      Forgotten Joint Score

    10. Satisfaction with knee surgery [Post-operatively at 6 weeks]

      Forgotten Joint Score

    11. Satisfaction with knee surgery [Post-operatively at 6 months]

      Forgotten Joint Score

    12. Satisfaction with knee surgery [Post-operatively at 1 year]

      Forgotten Joint Score

    13. Satisfaction with knee surgery [Post-operatively at 2 years]

      Forgotten Joint Score

    14. Function [post-operatively at 6 weeks]

      Oxford knee score

    15. Function [post-operatively at 6 months]

      Oxford knee score

    16. Function [pre-operatively]

      Oxford knee score

    17. Function [post-operatively at 2 years]

      Oxford knee score

    Other Outcome Measures

    1. Health Care Utilization [Post-operatively at 6 weeks]

      unanticipated visits to emergency department, primary care provide, surgeon due to knee surgery

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • undergoing unilateral TKR for the treatment of osteoarthritis

    • between the age of 18 and 85 years of age

    • able to read, speak and understand English, have a telephone

    • are able to provide consent

    Exclusion Criteria:
    • enrolled in another study, are

    • undergoing revision surgery or bilateral surgery, and are

    • over the age of 85 years. Patients will also be excluded if they

    • have a cognitive impairment (as indicated in the medical record) affecting their ability to comprehend the questions being asked

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 North York General Hospital Toronto Ontario Canada M2K 1E1

    Sponsors and Collaborators

    • North York General Hospital

    Investigators

    • Principal Investigator: Frank Mastrogiacomo, PhD, North York General Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Monakshi Sawhney, Clinical Professor, North York General Hospital
    ClinicalTrials.gov Identifier:
    NCT05490186
    Other Study ID Numbers:
    • NYGH REB #21-0043
    First Posted:
    Aug 5, 2022
    Last Update Posted:
    Aug 5, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 5, 2022