Prosthesis fixation / loosening
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with primary and secondary osteoarthritis who need a total hip prosthesis; Patients capable of giving informed consent and expressing a willingness to comply with the post-operative review program
Exclusion criteria
Exclusion criteria: Patients requiring revision arthroplasty; Patients with primairy bone disease The patient is unable or unwilling to sign the Patient Informed Consent (PIC) specific to this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pre-treatment evaluation will consist of clinical assessment, and medical history, functional evaluation (using different score forms) and by radiographic evaluation. After surgery evaluation will be performed on different intervals using measurements of RSA and functional evaluation (e.g. pain, work/activity level). | — |
Secondary
| Measure | Time frame |
|---|---|
| None | — |
Countries
Netherlands