TOTAL HIP REPLACEMENT M16
Conditions
Interventions
Group 1: Patients after primary Total Hip Replacement
Patient follow-up was according to defined time Points using X-ray and clinical investigation.
Sponsors
Ordensklinikum der barmherzigen Schwestern Linz
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All patients had primary osteoarthritis or avascular femoral head necrosis requiring THA. None had previous surgeries of the affected hip. All patients underwent primary total hip arthroplasty (THA) using a cement-less, short-stem design implant and a cement-less press-fit cup for osteoarthritis of avascular necrosis at our institution and had a minimum follow-up of 2 years.
Exclusion criteria
Exclusion criteria: Exclusion criteria were also arthroplasties in other joints in the lower limbs (total or unicompartmental knee, ankle), rheumatoid diseases, osteoporosis, malignant tumors, neurological diseases, bilateral THA or patients unable to participate in the study due to impaired health. Furthermore, we excluded patients who were not willing to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| THA (total hip arthroplasty) subsidence signs of loosening around stem/cup periostal reaction around stem/cup heterotopic ossification. All patients had radiological and clinical evaluation pre-operatively, within the first-postoperative week as well as 3, 12 and 24 months after index-surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| clinical Outcome | — |
Countries
Austria
Contacts
Public ContactJosef Hochreiter
Abteilung für Orthopädie Ordensklinikum Barmherzige Schwestern Linz
Outcome results
None listed