About this trial
The study will analyze hip biomechanical parameters using EOS radiographic measurements pre- and post-operatively (3 months) and post-operatively (3 months) CT scans after total hip replacement (THR), neck-preserving THR of the Minihip type or hip resurfacing (HR). Clinical results will be assessed at 3 months and 1 year after surgery.
To this end, two types of examination are carried out, both of which are used in current practice:
* Pre-operatively: EOS radiography * Post-operatively: EOS radiograph and CT scan
Inclusion (m-3; m-1) :
* Patient information at pre-operative visit * Non-opposition of patient, family member or legal guardian, if applicable * Questionnaires and clinical examination (standard management) * EOS during anesthetic consultation
Follow-up visit (m+3):
\- Post-operative follow-up consultation EOS and CT scan (1 week prior to visit) + questionnaire and clinical examination
Follow-up visit (m+12):
\- Post-operative check-up, questionnaire and clinical examination
Eligibility criteria
Qualifiers
Male or female
Age ≥ 18 years
Planned surgery: total hip arthroplasty, Minihip or RSA
Absence of osteoarthritis or osteoarthritis ≤ stage 1 (Tönnis classification) of contralateral hip (Radiographic analysis)
Disqualifiers
Anomalies or anatomical changes of the hip, pelvis or lumbar spine (history of fracture, protrusion, scoliosis, history of orthopedic surgery, dysplasia, torsion disorder)
Established genetic disease affecting the musculoskeletal system
Severe or morbid obesity
Neuromuscular pathologies affecting the limb girdles
Trial design
Treatments tested in this trial
- hip arthroplasty