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NitrX Total Knee Arthroplasty RSA

Primary Purpose

Total Knee Arthroplasty, Knee Osteoarthritis, Radiostereometric Analysis

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Total Knee Arthroplasty with Evolution® NitrX™ Knee System
Total Knee Arthroplasty with Evolution Knee System
Sponsored by
Lawson Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Total Knee Arthroplasty

Eligibility Criteria

21 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Symptomatic osteoarthritis of the knee indicating primary total knee arthroplasty
  • Varus knee deformity of 0 to 10 degrees
  • Sufficient ligamentous function to warrant retention of the posterior cruciate ligament
  • Between ages of 21 and 80 inclusive
  • Patients willing and able to comply with follow-up requirements and self-evaluations
  • Ability to give informed consent
  • No contraindications to Magnetic Resonance Imaging (MRI)

Exclusion Criteria:

  • Active or previous infection
  • Medical condition precluding major surgery
  • Inflammatory arthropathy
  • Prior Patellectomy
  • PCL deficiency
  • Major Coronal plane deformity
  • Valgus deformity
  • Bone defects requiring augments, cones and/or stemmed implants

Sites / Locations

  • London Health Sciences CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Evolution Total Knee Arthroplasty system

Evolution with NitrX Total Knee Arthroplasty system

Arm Description

Patients will undergo total knee arthroplasty with the Evolution Total Knee System

Patients will undergo total knee arthroplasty with the NitrX Evolution Total Knee System which has the specialized protective coating

Outcomes

Primary Outcome Measures

Implant Migration (Tibial Component)
Model based Radiostereometric Analysis (RSA, specialized Xrays) will be used to register the location of the tibial implant components during supine and standing exams and measure implant movement. Changes throughout the different time points of potential tibial migration, with the use of the tibial bone beads, will be measured in millimeters.

Secondary Outcome Measures

Implant Migration (Femoral Component)
Model based Radiostereometric Analysis (specialized Xrays) will be used to register the location of the femoral components during supine and standing exams and measure implant movement. Changes throughout the different time points of potential femoral migration, with the use of the femoral bone beads, will be measured in millimeters.

Full Information

First Posted
November 5, 2021
Last Updated
May 29, 2023
Sponsor
Lawson Health Research Institute
Collaborators
MicroPort Orthopedics Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05151315
Brief Title
NitrX Total Knee Arthroplasty RSA
Official Title
Component Migration, Polyethylene Wear, and Joint Inflammation of the Evolution Versus Evolution NitrX Total Knee Arthroplasty System
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2022 (Actual)
Primary Completion Date
April 30, 2024 (Anticipated)
Study Completion Date
November 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lawson Health Research Institute
Collaborators
MicroPort Orthopedics Inc.

4. Oversight

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.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Metal hypersensitivity is a recognized complication in some patients following total joint arthroplasty. This can result in a reaction to metal particles from the implants placed in the joint and cause tissue injury. The Evolution® NitrX™ (MicroPort Orthopaedics, Memphis, TN) knee implant was designed with the addition of a coating meant to create a barrier against the release of metal ions. The primary purpose of this study is to compare the Evolution and Evolution NitrX implant (implants your surgeon uses in total knee arthroplasty surgery). This study will compare the stability of these knee implants (any movement the implant makes after surgery) through the use of specialized xrays, called "radiostereometric analysis" (RSA for short). The investigators will also compare levels of circulating metal particles with blood draws and the effects of any circulating metal with MR imaging. The investigators will also be looking at the participants clinical outcomes using joint function and patient satisfaction questionnaires. A total of 50 patients will be enrolled into the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Total Knee Arthroplasty, Knee Osteoarthritis, Radiostereometric Analysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Evolution Total Knee Arthroplasty system
Arm Type
Active Comparator
Arm Description
Patients will undergo total knee arthroplasty with the Evolution Total Knee System
Arm Title
Evolution with NitrX Total Knee Arthroplasty system
Arm Type
Experimental
Arm Description
Patients will undergo total knee arthroplasty with the NitrX Evolution Total Knee System which has the specialized protective coating
Intervention Type
Device
Intervention Name(s)
Total Knee Arthroplasty with Evolution® NitrX™ Knee System
Intervention Description
Patients will receive cemented Evolution knee system with NitrX coating for their total knee arthroplasty.
Intervention Type
Device
Intervention Name(s)
Total Knee Arthroplasty with Evolution Knee System
Intervention Description
Patients will receive cemented Evolution knee system without NitrX coating for their total knee arthroplasty.
Primary Outcome Measure Information:
Title
Implant Migration (Tibial Component)
Description
Model based Radiostereometric Analysis (RSA, specialized Xrays) will be used to register the location of the tibial implant components during supine and standing exams and measure implant movement. Changes throughout the different time points of potential tibial migration, with the use of the tibial bone beads, will be measured in millimeters.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Implant Migration (Femoral Component)
Description
Model based Radiostereometric Analysis (specialized Xrays) will be used to register the location of the femoral components during supine and standing exams and measure implant movement. Changes throughout the different time points of potential femoral migration, with the use of the femoral bone beads, will be measured in millimeters.
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Wear Rates
Description
Model based Radiostereometric Analysis (specialized Xrays) will be used to register the location of the femoral and tibial components in both standing and supine exams where the minimum joint space width between components on the medial and lateral condyles can be calculated as a measurement (in millimeters) of polyethylene wear.
Time Frame
2 weeks (baseline), 6 weeks, 3 months, 6 months, 1 year, and 2 years.
Title
Circulating metal levels
Description
Patients will have blood drawn and the levels of circulating cobalt, chromium, and nickel will be measured in whole blood. One vial of blood will be drawn from the patient (in milliliters).
Time Frame
Pre-operative, 1 and 2 years post-operatively.
Title
Synovial Joint Inflammation observation
Description
Patients will complete an MRI exam using metal artefact reduction sequences. Scans will be evaluated and scored for synovial inflammation and fibrosis, indicative of reactions to metal debris, and the presence of fibrous tissue at the bone-cement-implant interface, indicative of component loosening.
Time Frame
2 Years
Title
Knee Injury and Osteoarthritis Outcome score (KOOS)
Description
Patient reported outcome measure. Holds 42 items that asks patient about pain, functional daily living, and sport and recreation. Questionnaire measures levels in frequency (never to always) and severity (none to extreme). Scores are from 0-100, with higher scores indicating no knee problems.
Time Frame
Pre-operative, 3 months, 1 year, and 2 year post-operative
Title
Forgotten Joint Score (FJS)
Description
Patient reported outcome measure observing the ability of a patient to forget about a joint due to successful treatment. Contains 12 items with frequency level measurement (never to mostly). The higher the score (0-100), the less aware the patient is of their affected joint when performing daily activity.
Time Frame
Pre-operative, 3 months, 1 year, and 2 year post-operative
Title
Veterans-Rand 12 Item Health Survey (VR-12)
Description
Patient reported outcome measure observing physical and mental health status of patient. Contains 14 items measuring levels of severity (excellent to poor) and frequency (None of the time to Yes, all of the time). Higher scores indicate higher quality of life and vice versa.
Time Frame
Pre-operative, 3 months, 1 year, and 2 year post-operative
Title
European Quality of Life - 5 Dimension (EQ-5D)
Description
Patient reported outcome measure. Standardized 5 item instrument measuring generic health status of patient. The EQ5D uses a Likert scale which assesses five states (mobility, self care, usual care, pain and discomfort and anxiety and depression) at five different levels - none(0), slight(1), moderate(2), severe(3) or unable to perform(5). Levels are coded 1-5 and an index score is then generated. Higher scores indicate higher health status of patient.
Time Frame
Pre-operative, 3 months, 1 year, and 2 year
Title
Metal Exposure/Sensitivity
Description
Patient reported outcome measure. Screening tool for noting pre-operative environmental metal exposures. Questionnaire contains Yes or No questions. Higher scores would indicate greater exposure and/or metal sensitivity.
Time Frame
Pre-operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Symptomatic osteoarthritis of the knee indicating primary total knee arthroplasty Varus knee deformity of 0 to 10 degrees Sufficient ligamentous function to warrant retention of the posterior cruciate ligament Between ages of 21 and 80 inclusive Patients willing and able to comply with follow-up requirements and self-evaluations Ability to give informed consent No contraindications to Magnetic Resonance Imaging (MRI) Exclusion Criteria: Active or previous infection Medical condition precluding major surgery Inflammatory arthropathy Prior Patellectomy PCL deficiency Major Coronal plane deformity Valgus deformity Bone defects requiring augments, cones and/or stemmed implants
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lyndsay Somerville, PhD
Phone
519 685 8500
Ext
36645
Email
lyndsay.somerville@lhsc.on.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Janel Dhooma, MPH
Phone
519 685 8500
Ext
32794
Email
janel.dhooma@lhsc.on.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edward M Vasarhelyi, MD
Organizational Affiliation
London Health Sciences Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Matthew Teeter, PhD
Organizational Affiliation
London Health Science Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
London Health Sciences Centre
City
London
State/Province
Ontario
ZIP/Postal Code
N6A5A5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Edward Vasarhelyi
Email
edward.vasarhelyi@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Lyndsay Somerville, PhD
Email
lyndsay.somerville@lhsc.on.ca
First Name & Middle Initial & Last Name & Degree
Edward Vasarhelyi, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29508661
Citation
Pijls BG, Plevier JWM, Nelissen RGHH. RSA migration of total knee replacements. Acta Orthop. 2018 Jun;89(3):320-328. doi: 10.1080/17453674.2018.1443635. Epub 2018 Mar 6.
Results Reference
background
PubMed Identifier
31038991
Citation
Teeter MG, Marsh JD, Howard JL, Yuan X, Vasarhelyi EM, McCalden RW, Naudie DDR. A randomized controlled trial investigating the value of patient-specific instrumentation for total knee arthroplasty in the Canadian healthcare system. Bone Joint J. 2019 May;101-B(5):565-572. doi: 10.1302/0301-620X.101B5.BJJ-2018-1323.R1.
Results Reference
background
PubMed Identifier
27143731
Citation
Teeter MG, Thoren J, Yuan X, McCalden RW, MacDonald SJ, Lanting BA, Naudie DD. Migration of a cemented fixed-bearing, polished titanium tibial baseplate (Genesis II) at ten years : a radiostereometric analysis. Bone Joint J. 2016 May;98-B(5):616-21. doi: 10.1302/0301-620X.98B5.36865.
Results Reference
background
PubMed Identifier
30562833
Citation
Teeter MG, Perry K, Yuan X, Howard JL, Lanting BA. The Effects of Resection Technique on Implant Migration in Single Radius Posterior-Stabilized Total Knee Replacement. J Knee Surg. 2020 Jan;33(1):78-83. doi: 10.1055/s-0038-1676462. Epub 2018 Dec 18.
Results Reference
background
Citation
Sealed Envelope Ltd.2012.Power calculator for continuous outcome non0-inferiority trial.[Online] Available from: https://www.sealedenvelope.com/power/continuous-noninferios/[Accessed Thu Jan 14 2021].
Results Reference
background
PubMed Identifier
24395396
Citation
van Ijsseldijk EA, Valstar ER, Stoel BC, de Ridder R, Nelissen RG, Kaptein BL. Measuring polyethylene wear in total knee arthroplasty by RSA: differences between weight-bearing and non-weight-bearing positioning. J Orthop Res. 2014 Apr;32(4):613-7. doi: 10.1002/jor.22579. Epub 2014 Jan 7.
Results Reference
background
PubMed Identifier
30794231
Citation
Teeter MG, Wihlidal J, McCalden RW, Yuan X, MacDonald SJ, Lanting BA, Naudie DD. Radiostereometric Analysis Permits In Vivo Measurement of Very Small Levels of Wear in TKA. Clin Orthop Relat Res. 2019 Jan;477(1):80-90. doi: 10.1097/CORR.0000000000000399.
Results Reference
background
PubMed Identifier
31674253
Citation
Gascoyne T, Parashin S, Teeter M, Bohm E, Laende E, Dunbar M, Turgeon T. In vivo wear measurement in a modern total knee arthroplasty with model-based radiostereometric analysis. Bone Joint J. 2019 Nov;101-B(11):1348-1355. doi: 10.1302/0301-620X.101B11.BJJ-2018-1447.R2.
Results Reference
background
PubMed Identifier
31975444
Citation
Koff MF, Burge AJ, Potter HG. Clinical magnetic resonance imaging of arthroplasty at 1.5 T. J Orthop Res. 2020 Jul;38(7):1455-1464. doi: 10.1002/jor.24606. Epub 2020 Feb 4.
Results Reference
background
PubMed Identifier
32993344
Citation
Attard V, Li CY, Self A, Mann DA, Borthwick LA, O'Connor P, Deehan DJ, Kalson NS. Quantification of intra-articular fibrosis in patients with stiff knee arthroplasties using metal-reduction MRI. Bone Joint J. 2020 Oct;102-B(10):1331-1340. doi: 10.1302/0301-620X.102B10.BJJ-2020-0841.R1.
Results Reference
background
PubMed Identifier
21741843
Citation
Heyse TJ, Chong le R, Davis J, Boettner F, Haas SB, Potter HG. MRI analysis of the component-bone interface after TKA. Knee. 2012 Aug;19(4):290-4. doi: 10.1016/j.knee.2011.05.011. Epub 2011 Jul 8.
Results Reference
background

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NitrX Total Knee Arthroplasty RSA

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