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Evaluation of Bone Mineral Density Changes Using Two Tibial Base Plate Designs in Primary Total Knee Arthroplasty in Young Patient

Primary Purpose

Knee Osteoarthritis

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Primary TKA with cemented modular metal-backed tibial implant
Primary TKA with uncemented trabecular metal
Sponsored by
Hopital du Sacre-Coeur de Montreal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis

Eligibility Criteria

45 Years - 59 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Tricompartmental osteoarthritis of the knee
  • Age, under 60 years old at the time of surgery
  • Stable health (the patient should be able to undergo surgery and participate in a follow-up program based upon physical examination and medical history).

Exclusion Criteria:

  • Diagnosis of inflammatory joint disease
  • Diagnosis of osteonecrosis
  • Infection; acute or chronic
  • Any current metal hardware on the proximal 25 cm of the tibia
  • History, remote or recent, of high tibial osteotomy or tibial plateau fracture
  • Any collateral ligamentous instability in the affected knee
  • Contra lateral below knee or above knee amputation
  • Ongoing Biphosphonate pharmacotherapy
  • Presence of clinically significant disease of the cardiovascular, renal, hepatic, hematologic,respiratory, endocrine, neurological, gastrointestinal, genitourinary, immune systems or other medical condition which is not well controlled.
  • Participants of a study who have received an investigational drug or device within the last 30 days
  • Patients unwilling or unable to cooperate in a follow-up program
  • Bone deficit (subchondral cyst)
  • Previous contralateral Total Knee Arthroplasty (TKA), ORIF, HTO
  • Patella deficiency needing grafting or preventing patella resurfacing

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Active Comparator

    Active Comparator

    Experimental

    Experimental

    Arm Label

    45-54 y.o / cemented modular metal-backed tibial implant

    55-59 y.o / cemented modular metal-backed tibial implant

    45-54 y.o / uncemented Trabecular Metal modular tibial implant

    55-59 y.o / uncemented Trabecular Metal modular tibial implant

    Arm Description

    This group will undergo a surgery for a knee arthroplasty following standard procedure at our center

    This group will undergo a surgery for a knee arthroplasty following standard procedure at our center

    This group will undergo a surgery for a knee arthroplasty with a trabecular metal of the tibial implant

    This group will undergo a surgery for a knee arthroplasty with a trabecular metal of the tibial implant

    Outcomes

    Primary Outcome Measures

    DEXA Scan
    This exam will quantify the amount of bone density at 24 months after total knee arthroplasty. DXA scan can provide accurate, high-quality measurements of periprosthetic bone mineral density (BMD) with minimal precision error and a low coeficient of variation ranging from 1.3% to 4.7%17.
    KOOS (knee injury and osteoarthritis outcomes score )
    The Index is self-administered and assesses the 5 subscales: pain (9 questions), other symptoms (7 questions), function in daily living (17 questions), function in sports and recreation (5) and knee related quality of live (4). All subscales are on 100, 100 being the best score, 0 the worst. The total score is an average of all subscale
    KSS (Knee Society Score)
    The original KSS has a "Knee Score" section (7 items) and a "Functional Score" section (3 items). Both sections are scored from 0 to 100 with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions.

    Secondary Outcome Measures

    The 12-item medical outcomes study short form health survey version 2.0 (SF-12v2)
    This self-administered generic health status measure is composed of 12 items measuring 3 major health attributes: functional status, well-being, and overall evaluation of health
    Lyshom and Tegner
    The Lysholm Scale currently consists of eight items that measure: pain (25 points), instability (25 points), locking (15 points), swelling (10 points), limp (5 points), stair climbing (10 points), squatting (5 points), and need for support (5 points). Every question response has been assigned an arbitrary score on an increasing scale. The total score is the sum of each response to the eight questions, and may range from 0-100. Higher scores indicate a better outcome with fewer symptoms or disability.

    Full Information

    First Posted
    May 27, 2019
    Last Updated
    February 17, 2020
    Sponsor
    Hopital du Sacre-Coeur de Montreal
    Collaborators
    Zimmer Biomet, CHU de Québec
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03970460
    Brief Title
    Evaluation of Bone Mineral Density Changes Using Two Tibial Base Plate Designs in Primary Total Knee Arthroplasty in Young Patient
    Official Title
    Randomized Clinical Evaluation of Bone Mineral Density Changes Using Two Tibial Base Plate Designs in Primary Total Knee Arthroplasty in Young Patients
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 5, 2011 (Actual)
    Primary Completion Date
    December 30, 2019 (Actual)
    Study Completion Date
    December 30, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Hopital du Sacre-Coeur de Montreal
    Collaborators
    Zimmer Biomet, CHU de Québec

    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
    Arthritic disease in people less than 60 years old is increasingly common. Younger, active individuals often present now to orthopaedic surgeons requiring treatment of knee osteoarthritis. Knee arthroplasty has been offered as a viable option to provide pain relief and improve function in the middle-aged patient. In a previous study submitted for publication, the investigators have looked at BMD in vivo after total knee replacement comparing two different tibial base plate designs in cemented and uncemented implants in terms of stiffness and modularity, and its effect on bone density changes, synovitis, osteolysis or survivorship. The investigators found a difference of 18% in bone mineral density favoring trabecular metal implant over cemented modular metal-back implant in patient between 55 and 75 years of age. The trabecular metal implant thus behaved as it was expected and preserved bone density in an elderly population. No randomized clinical trial has looked at cemented titanium tibial insert to uncemented trabecular metal tibia insert in young population. In order to isolate stiffness as study variable, one would aim at randomizing a homogeneous patient population undergoing total knee arthroplasty with implants of similar articular geometry designs with different tibial baseplate, titanium versus trabecular metal. The trabecular metal implant is closer to human bone modulus of elasticity.
    Detailed Description
    THE GOAL OF OUR STUDY IS TO Quantify the amount of bone remodeling 24 months after total knee arthroplasty using sequential dual-energy x-ray absorptiometry of the proximal tibia in younger and more active patients (less than 60 years of age). Evaluate the evolution of functional outcome over a 24 months period using sequential subjective and objective clinical evaluations using the Knee Society Score (KSS) and Knee Injury and Osteoarthritis Outcome Score (KOOS) and Sf-12 v2 in this cohort of patients. There is also an interest in looking at the activity level before and after the surgery (by using the Tegner Activity Level Scale and the UCLA Activity Level Scale) and to determine the ability to return to an active lifestyle and the impact on implant survival. Two groups will be created: Group 1: NexGen cemented modular metal-backed tibial implant (Titanium) Group 2: NexGen uncemented Trabecular Metal(TM) modular tibial implant A total of 88 patients will be recruited

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Knee Osteoarthritis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    88 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    45-54 y.o / cemented modular metal-backed tibial implant
    Arm Type
    Active Comparator
    Arm Description
    This group will undergo a surgery for a knee arthroplasty following standard procedure at our center
    Arm Title
    55-59 y.o / cemented modular metal-backed tibial implant
    Arm Type
    Active Comparator
    Arm Description
    This group will undergo a surgery for a knee arthroplasty following standard procedure at our center
    Arm Title
    45-54 y.o / uncemented Trabecular Metal modular tibial implant
    Arm Type
    Experimental
    Arm Description
    This group will undergo a surgery for a knee arthroplasty with a trabecular metal of the tibial implant
    Arm Title
    55-59 y.o / uncemented Trabecular Metal modular tibial implant
    Arm Type
    Experimental
    Arm Description
    This group will undergo a surgery for a knee arthroplasty with a trabecular metal of the tibial implant
    Intervention Type
    Device
    Intervention Name(s)
    Primary TKA with cemented modular metal-backed tibial implant
    Intervention Description
    Tibial implant will be done with a cemented implant
    Intervention Type
    Device
    Intervention Name(s)
    Primary TKA with uncemented trabecular metal
    Intervention Description
    Tibial implant will be done with a uncemented implant
    Primary Outcome Measure Information:
    Title
    DEXA Scan
    Description
    This exam will quantify the amount of bone density at 24 months after total knee arthroplasty. DXA scan can provide accurate, high-quality measurements of periprosthetic bone mineral density (BMD) with minimal precision error and a low coeficient of variation ranging from 1.3% to 4.7%17.
    Time Frame
    24 months post-op
    Title
    KOOS (knee injury and osteoarthritis outcomes score )
    Description
    The Index is self-administered and assesses the 5 subscales: pain (9 questions), other symptoms (7 questions), function in daily living (17 questions), function in sports and recreation (5) and knee related quality of live (4). All subscales are on 100, 100 being the best score, 0 the worst. The total score is an average of all subscale
    Time Frame
    2 years post-op
    Title
    KSS (Knee Society Score)
    Description
    The original KSS has a "Knee Score" section (7 items) and a "Functional Score" section (3 items). Both sections are scored from 0 to 100 with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions.
    Time Frame
    2 years post-op
    Secondary Outcome Measure Information:
    Title
    The 12-item medical outcomes study short form health survey version 2.0 (SF-12v2)
    Description
    This self-administered generic health status measure is composed of 12 items measuring 3 major health attributes: functional status, well-being, and overall evaluation of health
    Time Frame
    2 years post-op
    Title
    Lyshom and Tegner
    Description
    The Lysholm Scale currently consists of eight items that measure: pain (25 points), instability (25 points), locking (15 points), swelling (10 points), limp (5 points), stair climbing (10 points), squatting (5 points), and need for support (5 points). Every question response has been assigned an arbitrary score on an increasing scale. The total score is the sum of each response to the eight questions, and may range from 0-100. Higher scores indicate a better outcome with fewer symptoms or disability.
    Time Frame
    2 years post-op

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    45 Years
    Maximum Age & Unit of Time
    59 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Tricompartmental osteoarthritis of the knee Age, under 60 years old at the time of surgery Stable health (the patient should be able to undergo surgery and participate in a follow-up program based upon physical examination and medical history). Exclusion Criteria: Diagnosis of inflammatory joint disease Diagnosis of osteonecrosis Infection; acute or chronic Any current metal hardware on the proximal 25 cm of the tibia History, remote or recent, of high tibial osteotomy or tibial plateau fracture Any collateral ligamentous instability in the affected knee Contra lateral below knee or above knee amputation Ongoing Biphosphonate pharmacotherapy Presence of clinically significant disease of the cardiovascular, renal, hepatic, hematologic,respiratory, endocrine, neurological, gastrointestinal, genitourinary, immune systems or other medical condition which is not well controlled. Participants of a study who have received an investigational drug or device within the last 30 days Patients unwilling or unable to cooperate in a follow-up program Bone deficit (subchondral cyst) Previous contralateral Total Knee Arthroplasty (TKA), ORIF, HTO Patella deficiency needing grafting or preventing patella resurfacing
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michel Malo, ND
    Organizational Affiliation
    Hôpital Sacré-Coeur de Montréal
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Evaluation of Bone Mineral Density Changes Using Two Tibial Base Plate Designs in Primary Total Knee Arthroplasty in Young Patient

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