M16 M87.05 M87.35
Conditions
Interventions
Group 1: Clinical and radiological follow up in patients with Spiron total hip arthroplasty is done three months and one year postoperatively, then yearly and compared to preoperative status.
The pat
Sponsors
Johannes Wesling Klinikum Minden
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: primary or secondary osteoarthritis of the hip, femoral head necrosis
Exclusion criteria
Exclusion criteria: pathologic geometry of the hip (short femoral neck, CCD-angle >150°, CCD-angle <120°), destructed or discontinued femoral neck, manifest osteoporosis, ongoing chemotherapy, pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| One year postoperative the following primary endpoints are assessed: patient satisfaction: nineary scale; pain relief: visual-analogue-scale; hip joint function: Harris-Hip-Score, Oxford-Hip-Score; life quality: Short form 36, EQ-5D; radiological assessment: X-ray of the pelvis and cross-table view of the hip. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints: prosthetic loosening, revision surgery of any kind. Yearly examination of the incidence of the secondary endpoints and implementation of a Kaplan-Meier-calculation. End of observation: 10 years following hip arthroplasty. | — |
Countries
Germany
Contacts
Public ContactArmin Lugeder
Johannes Wesling Klinikum Minden
Outcome results
None listed