Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation

Osteoarthritis of Knee Clinical Trial

Official title:

Total Knee Replacement Component Alignment Using Manual Versus Custom Instrumentation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02579174
• Other study ID #: STU00200223
• Status: Completed
• Phase: N/A
• Start date: January 2015
• Est. completion date: November 30, 2020

Study information

• Verified date: October 2022
• Source: Northwestern University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 112
• Est. completion date: November 30, 2020
• Est. primary completion date: September 8, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

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

Related Conditions & MeSH terms

• Osteoarthritis of Knee
• Osteoarthritis, Knee

Intervention

Device:
• Medacta GMK Sphere

Locations

Country	Name	City	State
United States	Northwestern Medicine Department of Orthopaedic Surgery	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	Pre-operative, 6 wks. post-op
Secondary	Tibial Varus Deformity	Measured change between pre-operative planning report & post-operative EOS longstanding radiograph in varus deformity of the operative joint	Pre-operative, 6 wks. post-op
Secondary	Femoral Valgus Deformity	Measured change between pre-operative planning report & post-operative EOS longstanding radiograph in varus deformity of the operative joint	Pre-operative, 6 wks. post-op
Secondary	Tibial Posterior Slope (Mean Deviation)	Deviation from pre-operative planning template & 6 wk. post-operative longstanding EOS radiograph	Pre-Operative - 6 wk. Post-Operative