Totale heuparthroplastiek Total hip artroplasty total hip replacement
Conditions
Interventions
Sponsors
Philips Research
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: Patients with a unilateral or bilateral THA replacement.
Exclusion criteria
Exclusion criteria: - No written informed consent - Patient not meeting the inclusion criteria - Previous participation in the study - Pregnant women - Concomitant participation in a study in which the patient is exposed to X-rays - Patients younger than 40 years old
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main study parameters/endpoints: The main study parameters are a current standard care CT scan and an additional low-dose CT scan with 20%, 40%, 60% or 80% lowered radiation dose. The main endpoints are the objective and subjective image quality at different radiation dose levels for iterative reconstruction and model-based iterative reconstruction. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters are metal artefacts. The secondary endpoints are objective and subjective image quality in conventional non-O-MAR images and O-MAR images. | — |
Countries
The Netherlands
Outcome results
None listed