Multicenter Study for Robotic Arm-assisted THA 4.0 System: Hip Spine Relationship
NCT ID: NCT04646096
Last Updated: 2025-01-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
35 participants
INTERVENTIONAL
2021-01-01
2024-10-10
Brief Summary
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Detailed Description
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In conjunction with numerous other patient-specific and surgical factors, such as age, sex, comorbidities, surgical approach, component selection, and impingement, component positioning is often cited as an important factor in optimizing THA stability. Lewinnek et al. defined the "safe zone" for component position as 40⸰±10⸰ of cup inclination and 15⸰±10⸰ of cup anteversion to minimize dislocation risk. However, recent studies have shown that not only do components continue to dislocate when placed in this zone, but that the majority of THA dislocations are positioned in this safe zone to begin with. Compounding this issue is the growing body of evidence showing that the acetabular component is not static in nature, as was the assumption with Lewinnek's safe zone, but rather dynamically changing with movement of the pelvis and spine during postural and positional changes. Alterations of the dynamic relationship between the hip, spine, and pelvis in patients with hip-spine pathology during movements such as transitioning from standing to sitting affects typical pelvic biomechanical accommodation, resulting in THA component impingement, instability, and dislocation. Therefore, patients with spinopelvic pathology secondary to arthritis, spinal fusion, or spinal deformity are more prone to dislocation and revision following primary THA. The standard modality for assessing hip component position postoperatively is a 2D anteroposterior radiograph, due to low radiation dose and low cost. However, hip replacement components are placed in a 3-dimensional pelvis and femur, and therefore an anteroposterior radiograph alone may not give accurate information on the anteversion of the acetabular or femoral component. Studies have shown that cup anteversion measured with radiographs can have serious deviations with a substantial error range (mean deviation +1.74°, range -16.6° to 29.8°). This is attributed to the fact that radiographs cannot control for pelvic rotation and/or tilt. Recently a limited number of studies have started to use the other imaging modalities for understanding pelvic tilt in patients undergoing hip arthroplasty.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Mako THA 4.0 group
Hip system used: femoral stem (Accolade II), acetabular cup (Trident II or MDM if necessary), femoral head (ceramic or metal head compatible with Accolade II), acetabular insert (X3 Trident II or MDM liner when using MDM cup). Mako THA 4.0 software also will be used.
MAKO THA 4.0 System
Measure how the accuracy and precision of robotic arm-assisted total hip arthroplasty (THA) for placement accuracy of implant position in both the anterior and posterior approach.. The intervention will assess the precision of the MAKO system in placing hip components according to plan. It will compare hip angles executed by the Mako system intraoperatively with the 'gold standard' of 3D computer tomography (CT) scans.
The postoperative CT scan can show the precision of the MAKO system by accurately determining the location of hip replacements in patients after surgery.
Interventions
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MAKO THA 4.0 System
Measure how the accuracy and precision of robotic arm-assisted total hip arthroplasty (THA) for placement accuracy of implant position in both the anterior and posterior approach.. The intervention will assess the precision of the MAKO system in placing hip components according to plan. It will compare hip angles executed by the Mako system intraoperatively with the 'gold standard' of 3D computer tomography (CT) scans.
The postoperative CT scan can show the precision of the MAKO system by accurately determining the location of hip replacements in patients after surgery.
Eligibility Criteria
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Inclusion Criteria
* Willing and able to comply with postoperative follow up requirements
* at least 18 years of age
* sign an IRB approved informed consent
Exclusion Criteria
* Skeletally immature
* patient with active infection or suspected latent infection in or about joint
* bone stock inadequate for support or fixation of the prosthesis
* Neuromuscular disorders, muscle atrophy, or vascular deficient in the affected limb
* Ankylosing spondylitis
18 Years
ALL
No
Sponsors
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Stryker Orthopaedics
INDUSTRY
Hospital for Special Surgery, New York
OTHER
American Hip Institute
OTHER
Responsible Party
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Benjamin Domb, MD
Medical Doctor
Principal Investigators
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Benjamin G Domb, MD
Role: PRINCIPAL_INVESTIGATOR
American Hip Institute
Locations
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American Hip Institute
Des Plaines, Illinois, United States
Countries
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References
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Nodzo SR, Chang CC, Carroll KM, Barlow BT, Banks SA, Padgett DE, Mayman DJ, Jerabek SA. Intraoperative placement of total hip arthroplasty components with robotic-arm assisted technology correlates with postoperative implant position: a CT-based study. Bone Joint J. 2018 Oct;100-B(10):1303-1309. doi: 10.1302/0301-620X.100B10-BJJ-2018-0201.R1.
Other Identifiers
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AHI-003
Identifier Type: -
Identifier Source: org_study_id
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