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Optimization of prosthesis planning using a digital X-ray system (EOS)

Conditions
M16.9
Coxarthrosis, unspecified
Registration Number
DRKS00015053
Lead Sponsor
Orthopädische Universitätsklinik Friedrichsheim gGmbH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients diagnosed to have a cementless hip arthroplasty, free walking and standing without support.

Exclusion Criteria

• BMI = 30
• previous endoprosthetic interventions (ipsilateral and contralateral hip, knee and ankle joints)
• Surgical interventions on the musculoskeletal system during the previous 6 months.
• ASA-Klassifikation > 2
• progressive joint inflammation or destructive rheumatoid arthritis
• Neurologic diseases (z.B. Morbus Parkinson, stroke with paralysis, Muscular dystrophy, Epilepsy, Multiple Sclerosis, Paraneoplastic Neurologic Syndrom (PNS), Tremor, Alzheimer's disease, Huntington's chorea, Polio, cerebral palsy)
• injuries of the lower extremities
• no informed consent
• Patients with x-ray images which can be used for planning.
• Patients who can not stand still for about 10 seconds as one of the requirements for EOS

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The prosthetic sizes (cup and stem size) predicted with the TraumaCad® software in the one group and with the hipEOS software for the other group will be compared to the actual implanted sizes.
Secondary Outcome Measures
NameTimeMethod
1. The correlations between the static situation, defined by leg length discrepancy, degree of leg misalignment and degree of rotational deformity (calculated by SterEOS® on the postoperative EOS image), and the dynamics of gait (defined by joint loads, spatial-temporal parameters and range of motion).<br>2. COMP concentration from the blood samples.
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