Measured vs Navigated Techniques in Total Hip Arthroplasty
Accuracy in aChieving Optimum reconstrUction: Measured- vs. Navigation- Techniques in Hip Arthroplasty
1 other identifier
interventional
100
0 countries
N/A
Brief Summary
Accurate reconstruction of the native hip parameters following total hip arthroplasty is associated with improved outcome. In order to improve ability for optimum reconstruction, 3-D templating software can be utilized that provide detailed information regarding native anatomy. In order to achieve reconstruction within acceptable parameters as per pre-operative plan, some surgeons propose the use of intra-operative devices that measure component orientation and joint reconstruction ("Measured-THA"), whilst others propose the use of navigation tools ("Navigation-THA). Both techniques have shown superiority compared to the most commonly used "freehand" technique, but no prior study has assessed for superiority between these 2 techniques. Furthermore, to-date assessment of post-operative reconstruction has not been tested in detail as post-THA assessments are based on radiographs which provide incomplete, 2-dimensional, assessments and are lacking the important axial plane reconstruction parameters. The aims of this prospective, randomized, trial are to 1. appraise the ability to achieve the pre-operative 3-D plan (as per FormusLab) through a comparison of pre-op plan to post-operative reconstruction; 2. compare ability to accurately reconstruct hip following THA between "navigated-" (IntelliJoint®) and "measured-" techniques; and in doing so it will also 3. assess the accuracy of the intra-operative assessments of reconstruction through a comparison of objective (i.e. measured) intra-operative assessments with the post-operative reconstructions achieved.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2022
Typical duration for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 10, 2021
CompletedFirst Posted
Study publicly available on registry
May 26, 2022
CompletedStudy Start
First participant enrolled
July 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2024
CompletedMay 26, 2022
May 1, 2022
2 years
December 10, 2021
May 25, 2022
Conditions
Outcome Measures
Primary Outcomes (4)
Change in Pain Assessment - Oxford Hip Score
The Oxford Hip Score will be given to patients to assess subjective measures of hip pain. Scores for each question from 0 to 4 with 4 being the best outcome. This method, when summed, produces overall scores running from 0 to 48 with 48 being the best outcome
once pre-operatively and once one-year post-operatively
Change in mobility, self-care, usual activities, pain/discomfort and anxiety/depression- EuroQol
the EuroQol (EQ-5D-5L) will be given to patients to assess subjective measures mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension in the EQ-5D-5L has five response levels: no problems (Level 1); slight; moderate; severe; and extreme problems (Level 5). The maximum score of 1 indicates the best health state, by contrast with the scores of individual questions, where higher scores indicate more severe or frequent problems.
once pre-operatively and once one-year post-operatively
Change in physical, mental, and social health- PROMIS Global-10
the PROMIS Global-10 will be given to patients to assess subjective measures of physical, mental and social health. It is a 10-item patient-reported questionnaire in which the response options are presented as 5-point (as well as a single 11-point) rating scales. The results of the questions are used to calculate two summary scores: a Global Physical Health Score and a Global Mental Health score. Higher scores indicate worse physical and mental health
once pre-operatively and once one-year post-operatively
Adverse Events
Serious adverse events will be monitored. This includes: * Wound complication * Dislocation * Fracture * Infection * Re-operation * Revision surgery
90 days post-operatively
Secondary Outcomes (4)
Accuracy of reconstruction (in mm)
post-operatively (within one week post-operatively)
Comparison of margin of error
Through study completion, an average of 1 year
Accuracy of reconstruction on outcome
Through study completion, an average of 1 year
Accuracy of reconstruction (in degrees)
post-operatively (within one week post-operatively)
Study Arms (2)
Measured Technique
EXPERIMENTALPatients in this group will have pre-operative planning done using the measured technique.
Navigated Technique
EXPERIMENTALPatients in this group will have pre-operative planning done using the navigated technique.
Interventions
Manual intra-operative checks and tools are used to aid in component placement during surgery.
IntelliJoint® navigation is an imageless-based navigation system that utilizes a miniature infrared camera and microelectronics to measure hip center of rotation, acetabular inclination and version, leg length, and offset. The device provides accurate real-time data on implant positioning to aid in placement of the components during surgery.
Eligibility Criteria
You may qualify if:
- Patients who are signed for a THA for primary or secondary osteoarthritis without overt deformity that would require revision type implants and with good enough bone quality to be listed for uncemented component implantation.
You may not qualify if:
- Secondary OA due to Dysplasia (Hartofilakidis \>1)
- Avascular necrosis of the hip with destruction of joint structure
- Sequelae of Pediatric deformity with abnormal anatomy
- Cemented fixation of femur or acetabulum
- Previous arthroplasty-type procedure
- Previous septic arthritis of the hip
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ottawa Hospital Research Institutelead
- FormusLabcollaborator
Related Publications (39)
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BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
George Grammatopoulos, MD
The Ottawa Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 10, 2021
First Posted
May 26, 2022
Study Start
July 1, 2022
Primary Completion
July 1, 2024
Study Completion
September 1, 2024
Last Updated
May 26, 2022
Record last verified: 2022-05