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Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation

Primary Purpose

Osteoarthritis of Knee

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Medacta GMK Sphere
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis of Knee

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Radiographically confirmed diagnosis of osteoarthritis (OA)
  • Failure of non-operative treatment for the diagnosis of symptomatic osteoarthritis
  • Age greater than 18 years
  • Desire to proceed with elective TKR
  • Completion of informed consent and signature of written consent form

Exclusion Criteria:

  • Ligamentous instability that may necessitate a constrained TKR implant
  • Retained hardware in the distal femur or proximal tibia of the operative extremity
  • Medical contraindication to undergo preoperative CT, or inability to tolerate preoperative CT

Sites / Locations

  • Northwestern Medicine Department of Orthopaedic Surgery

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Other

Other

Other

Arm Label

Manual (tibia) and manual (femur)

Manual (tibia) and custom (femur)

Custom (tibia) and custom (femur)

Custom (tibia) and manual (femur)

Arm Description

Knee replacement with Medacta GMK Sphere implants using manual instrumentation for both the tibia component and the femur component

Knee replacement with Medacta GMK Sphere implants using manual instrumentation for the tibia component and custom instrumentation for the femur component

Knee replacement with Medacta GMK Sphere implants using custom instrumentation for both the tibia component and the femur component

Knee replacement with Medacta GMK Sphere implants using custom instrumentation for the tibia component and manual instrumentation for the femur component

Outcomes

Primary Outcome Measures

Post-Operative Hip-Knee-Angle (HKA)
Measured HKA change from pre-operative EOS longstanding X-ray to post-operative EOS at 6wks. comparing groups receiving manual instrumentation versus custom instrumentation

Secondary Outcome Measures

Tibial Varus Deformity
Measured change between pre-operative planning report & post-operative EOS longstanding radiograph in varus deformity of the operative joint
Femoral Valgus Deformity
Measured change between pre-operative planning report & post-operative EOS longstanding radiograph in varus deformity of the operative joint
Tibial Posterior Slope (Mean Deviation)
Deviation from pre-operative planning template & 6 wk. post-operative longstanding EOS radiograph

Full Information

First Posted
October 13, 2015
Last Updated
October 24, 2022
Sponsor
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT02579174
Brief Title
Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation
Official Title
Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
September 8, 2020 (Actual)
Study Completion Date
November 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
To determine whether the low-dose, biplanar x-ray imaging (EOS) has the same accuracy as computed axial tomography (CT) To validate low-dose, biplanar x-ray imaging (EOS) as a tool to evaluate 3-dimensional alignment of Total Knee Replacement implants. To evaluate differences in total knee replacement implant alignment in patients whose arthroplasty is performed using manual or custom instrumentation derived from preoperative CT
Detailed Description
Achieving optimal prosthetic alignment of the femoral, tibial and patellar components during Total Knee Replacement (TKR) is of great importance as it contributes to better function, less pain and improved quality of life.TKR requires accuracy in the execution of bone cuts in the correct orientation to the coronal, sagittal and axial planes. Malposition potentially leads to increased mechanical stress on the bearing surfaces and inevitably to earlier loosening. Computed Axial Tomography (CT) is the gold standard technique to evaluate implant alignment in the coronal, sagittal and axial planes. As such, CT has imaging has been used to create custom instrumentation with purported likely improvement in surgical outcomes. Customized instrumentation created from a preoperative CT has been shown to be safe and effective, with no reported difference in patient outcomes and similar total knee arthroplasty component alignment. However, taking into consideration CT's high levels of radiation, cost expenses and its inability to obtain images of the limb in weight-bearing position, CT scan cannot be used routinely as a postoperative tool to evaluate TKR implant positioning. The imaging system manufactured by EOS Imaging (formerly Biospace Med, Paris) is a biplanar, low-dose radiation, full body, high resolution, radiological imaging system allowing simultaneous acquisition in the coronal and sagittal planes and in standing position.EOS' main benefits are the considerable reduction in radiation dose (up to 1000 times less than for CT and ten times less than the plain radiography) by using a gaseous detector. George Charpak, the inventor, was awarded the Nobel Prize in 1992 for this work. Moreover, the EOS system can provide 3D images by using the appropriate software algorithms, thus providing a low-radiation alternative to CT.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Participant
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Manual (tibia) and manual (femur)
Arm Type
Other
Arm Description
Knee replacement with Medacta GMK Sphere implants using manual instrumentation for both the tibia component and the femur component
Arm Title
Manual (tibia) and custom (femur)
Arm Type
Other
Arm Description
Knee replacement with Medacta GMK Sphere implants using manual instrumentation for the tibia component and custom instrumentation for the femur component
Arm Title
Custom (tibia) and custom (femur)
Arm Type
Other
Arm Description
Knee replacement with Medacta GMK Sphere implants using custom instrumentation for both the tibia component and the femur component
Arm Title
Custom (tibia) and manual (femur)
Arm Type
Other
Arm Description
Knee replacement with Medacta GMK Sphere implants using custom instrumentation for the tibia component and manual instrumentation for the femur component
Intervention Type
Device
Intervention Name(s)
Medacta GMK Sphere
Primary Outcome Measure Information:
Title
Post-Operative Hip-Knee-Angle (HKA)
Description
Measured HKA change from pre-operative EOS longstanding X-ray to post-operative EOS at 6wks. comparing groups receiving manual instrumentation versus custom instrumentation
Time Frame
Pre-operative, 6 wks. post-op
Secondary Outcome Measure Information:
Title
Tibial Varus Deformity
Description
Measured change between pre-operative planning report & post-operative EOS longstanding radiograph in varus deformity of the operative joint
Time Frame
Pre-operative, 6 wks. post-op
Title
Femoral Valgus Deformity
Description
Measured change between pre-operative planning report & post-operative EOS longstanding radiograph in varus deformity of the operative joint
Time Frame
Pre-operative, 6 wks. post-op
Title
Tibial Posterior Slope (Mean Deviation)
Description
Deviation from pre-operative planning template & 6 wk. post-operative longstanding EOS radiograph
Time Frame
Pre-Operative - 6 wk. Post-Operative

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Radiographically confirmed diagnosis of osteoarthritis (OA) Failure of non-operative treatment for the diagnosis of symptomatic osteoarthritis Age greater than 18 years Desire to proceed with elective TKR Completion of informed consent and signature of written consent form Exclusion Criteria: Ligamentous instability that may necessitate a constrained TKR implant Retained hardware in the distal femur or proximal tibia of the operative extremity Medical contraindication to undergo preoperative CT, or inability to tolerate preoperative CT
Facility Information:
Facility Name
Northwestern Medicine Department of Orthopaedic Surgery
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

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Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation

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