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TKA Using Patient-Specific Instrumentation

Primary Purpose

Knee Osteoarthritis

Status
Withdrawn
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Stryker ShapeMatch Technology
Stryker Triathlon Custom Fit Knee
Sponsored by
Queen's University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged = 50-75
  • BMI = 20 - 40
  • Preoperative ability to perform certain gait tasks/skills
  • No previous knee surgery or injury on either limb
  • No neuromuscular disease or neurologic disease
  • ASA of 1-2

Exclusion Criteria:

  • below age 50 and/or above age 75
  • BMI less than 20 or greater than 40
  • ASA of 3 or higher

Sites / Locations

  • Hotel Dieu Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Stryker Triathlon Custom Fit Knee

Stryker shape match

Arm Description

implanted in standard fashion

no longer RCT

Outcomes

Primary Outcome Measures

gait analysis
Treadmill walk

Secondary Outcome Measures

Full Information

First Posted
April 7, 2014
Last Updated
April 4, 2018
Sponsor
Queen's University
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1. Study Identification

Unique Protocol Identification Number
NCT03117959
Brief Title
TKA Using Patient-Specific Instrumentation
Official Title
A Randomized Control Trial Comparing an Anatomical Axis Aligned and Conventional Mechanical Axis Total Knee Arthroplasty Using Patient-Specific Instrumentation
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Withdrawn
Why Stopped
no longer RCT - same surgical technique and implant used
Study Start Date
February 2014 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of our study is to determine if anatomic/kinematic total knee arthroplasties (TKAs) are superior to mechanical axis-referenced TKAs with respect to determinants of gait functionality, patient satisfaction and other objective tests of knee function as a potential indicator of long-term prosthesis outcomes. To our knowledge there has not been any literature comparing TKAs using the kinematic and mechanical axes with respect to gait analysis. A single study has compared gender-specific TKAs and found that there is no difference with respect to determinants of gait when using these prostheses (Thomsen et al, 2012), but again this study was not based on referencing off of the anatomical/kinematic axis of the knee. Our group is hoping that the small variability that may be detectable with the precision of gait analysis may be used as a predictor of future prosthesis outcome measures.
Detailed Description
The reference standard for total knee replacement or total knee arthroplasty (TKA) has historically been based on a 2-dimensional "mechanical axis" of the knee which surgically creates a joint line parallel to the ground. This is based on the idea that this alignment will evenly distribute the stress on the prosthesis, thus improving the wear characteristics and longevity of the replacement. More recent studies have shown that TKAs with greater than 3 degree deviation (in either valgus or varus) from this previously accepted ideal does not convey a survival benefit over a 15 year period. This is not to say that alignment does not play a role in survivorship as gross deviation from neutral does result in earlier implant failure, but a simple 2-D model may not be the ideal approach to TKAs. With the developments and improvements in patient-specific technology (or patient-specific instrumentation (PSI)), our ability to create TKAs that reproduce the patient's original anatomic or kinematic alignment in 3-Dimensions has dramatically improved. Early research with respect to function and survivorship has shown that PSIs are at least equivalent when compared to conventional TKAs. Some studies have also suggested improvements with respect to shorter operating times, less blood loss and increased range of motion. Most of the current PSI TKA literature has placed an emphasis on the technology's effect on TKA alignment or to show that it is bioequivalent with respect to range of motion or early prosthesis survivorship when compared to conventional TKAs. Although a single study using PSIs (Howell et al., 2013) has shown improvement in Oxford Knee Scores when comparing patients preoperatively to postoperatively, to our knowledge there is no research done to directly compare the functional knee scores between a mechanically-aligned and anatomically aligned TKA. This randomized control trial will compare these two approaches using implants from the same manufacturer and also hope to identify more subtle functional differences using power testing and gait analysis, in addition to assessing other perioperative outcomes such as blood loss, hospital stay duration and operative time.

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
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Stryker Triathlon Custom Fit Knee
Arm Type
Placebo Comparator
Arm Description
implanted in standard fashion
Arm Title
Stryker shape match
Arm Type
Experimental
Arm Description
no longer RCT
Intervention Type
Device
Intervention Name(s)
Stryker ShapeMatch Technology
Intervention Description
Will use this patient-specific guide for alignment with Stryker Triathlon Custom Fit Knee.
Intervention Type
Device
Intervention Name(s)
Stryker Triathlon Custom Fit Knee
Primary Outcome Measure Information:
Title
gait analysis
Description
Treadmill walk
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged = 50-75 BMI = 20 - 40 Preoperative ability to perform certain gait tasks/skills No previous knee surgery or injury on either limb No neuromuscular disease or neurologic disease ASA of 1-2 Exclusion Criteria: below age 50 and/or above age 75 BMI less than 20 or greater than 40 ASA of 3 or higher
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gavin Wood, MD
Organizational Affiliation
Queen's University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hotel Dieu Hospital
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 5G2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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TKA Using Patient-Specific Instrumentation

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