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Clinical Trials/NCT02579174
NCT02579174
Completed
Not Applicable

Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation

Northwestern University1 site in 1 country112 target enrollmentJanuary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis of Knee
Sponsor
Northwestern University
Enrollment
112
Locations
1
Primary Endpoint
Post-Operative Hip-Knee-Angle (HKA)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

  1. To determine whether the low-dose, biplanar x-ray imaging (EOS) has the same accuracy as computed axial tomography (CT)
  2. To validate low-dose, biplanar x-ray imaging (EOS) as a tool to evaluate 3-dimensional alignment of Total Knee Replacement implants.
  3. 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.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
November 30, 2020
Last Updated
3 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

David W. Manning

Associate Professor

Northwestern University

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

Outcomes

Primary Outcomes

Post-Operative Hip-Knee-Angle (HKA)

Time Frame: Pre-operative, 6 wks. post-op

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 Outcomes

  • Tibial Posterior Slope (Mean Deviation)(Pre-Operative - 6 wk. Post-Operative)
  • Tibial Varus Deformity(Pre-operative, 6 wks. post-op)
  • Femoral Valgus Deformity(Pre-operative, 6 wks. post-op)

Study Sites (1)

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