Osteoarthritis
Conditions
Keywords
Radiostereometric Analysis (RSA), Total hip arthroplasty (THA), Hip anatomy, Hip biomechanics
Brief summary
The purpose of this prospective, randomized study is to evaluate the importance of restoring the exact individual hip biomechanics during total hip arthroplasty.
Detailed description
This prospective, controlled and randomized study aims at evaluating the correlation between postoperative hip prosthesis migration and the achieved exactness of biomechanical restoration of hip mechanics during total hip arthroplasty (THA). The main objective is to find out how close the result from the surgery can come to a preferred prosthesis position and whether this makes any difference in terms of loosening, functionality and quality of life for the patient. The prosthesis positioning is performed with either (1) computer assisted navigation, (2) instrumented hip guide measuring devise alignment technique or (3) conventional non-instrumented measuring technique. The ABG II stem system (Stryker) will be used in the modular version for group 1 and 2 and the non-modular version in group 3. Before each operation the investigators will perform exact measurements of anatomical variables using preoperative radiographs (maximum 8 weeks old) and computed tomography images (CT)(taken 3-4 weeks preoperatively). While applying these measurements the investigators will try to preserve the patient´s individual biomechanical situation, most often as compared to the healthy contralateral hip. The variables to be analysed are anteversion of the femoral neck, offset and leg length. This preoperative hip analysis combined with the use of a templating system will give the data needed for component choice and exact positioning of the ABG II hip prosthesis. 75 patients will be randomized into the three groups (25+25+25). The patients will be followed with RadioStereometric Analysis (RSA) for two years (directly postoperatively, 14 days, 3 months, 1 year and 2 years). There will be a second CT scan 1 year postoperatively to measure the actual achieved position. In completion hip specific and general health questionnaires will be used to evaluate patient satisfaction and outcome. All patients will be subject to 3-Dimensional (3-D) gait analysis 3-4 weeks prior to surgery and after one year. The results of the gait analysis will be correlated to the achieved restoration of the hip anatomy and biomechanics. The investigators aim is to improve the fundamental understanding of the hip biomechanics in patients undergoing THA. Will physical performance improve when the individual hip biomechanics is better restored, and in which way and to what extent?
Interventions
PROCEDUREGF hip guide
Using GF hip guide to measure and control the peroperative positioning of the hip stem
PROCEDUREStryker Navigation System
Using Orthomap Modular Hip Software to navigate the operation
DEVICEABG II modular femoral component
A hip prosthesis made by Stryker. It has the same basic shape as the ABG II femoral component but has a modular neck system allowing it to better follow the patient specific hip anatomy regarding offset, varus-valgus angle and rotation in the anteroposterior plane.
Sponsors
Region Skane
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Osteoarthritis (OA) of the hip necessitating primary total hip arthroplasty (THA) * Male and non-pregnant female patients * Hip bone quality and morphology suitable for uncemented THA * Age up to 75 years old at the inclusion time of the study * Patients who understand the conditions of the study and are willing to participate for the length of the prescribed follow-up. * Patients who are capable of, and have given informed consent for participation in the study.
Exclusion criteria
* Rheumatoid arthritis * Malignant disease * Severe osteoporosis * Patients with active infection * Patients with malignancy * Prior major surgery in the hip to be operated on * Peroperative fracture * Hip prosthesis or grossly distorted hip anatomy in the contralateral hip. * Ongoing corticosteroid (oral) or immunosuppressive medication * Personal disorders (dementia, alcohol or drug abuse etc) suspected of making completion of the trial uncertain. * Patients with concurrent illnesses which are likely to affect their outcome.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Radiostereometric Analysis (RSA) | First postoperative day(reference examination), 14 days, 3 months, 1 and 2 years | This will measure the change in migration (translation and rotation around the x-, y- and z-axis of the hip) over time from baseline which is the direct postoperative examination and up to 2 years postoperatively. The migration pattern over a 2-year period can predict the long-term fate of the prosthesis |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Gait analysis | Preoperatively (3-4 weeks) and 1 year postoperatively | This will measure how the patients gait pattern has changed from preoperatively when the patient had symptoms from osteoarthritis and 1 year postoperatively when everything has healed and the new hip prosthesis should have full effect on function and pain relive. |
| Computer Tomography (CT) | Preoperatively (3-4 weeks) and 1 year postoperatively | This will measure how much the anatomy has changed from preoperatively to after the new hip prosthesis has been put in. Are the goals of hip anatomy restoration achieved? The main measurements will be leg length, global offset and rotation of femoral neck. |
| General and hip specific health questionnaires | preoperatively (3-4 weeks), 1 and 2 years postoperatively | Hip disability and Osteoarthritis Outcome Score (HOOS) - this is a hip specific questionnaire that will measure how the operation has affected the patients function and pain situation over time. EuroQol (EQ-5D) - a standardized instrument for use as measure of general health outcome over time |
Countries
Sweden
Outcome results
None listed