Patiënten die doorverwezen worden voor CT-hart (indicatie: hart en vaatziekten), CT-thorax (indicatie: follow-up voor longnodules), CT-abdomen (indicatie: follow-up voor nierstenen) en CT-enkel. Not applicable
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Cardiac CT: * * 50 years old * The indication for the CT-scan is suspected cardiovascular disease * Written informed consent;Chest CT: * * 50 years old * Patients with one or more known pulmonary nodules * The indication for the CT-scan is follow-up of one or more pulmonary nodules * Written informed consent;Abdominal CT: * * 40 years old * The indication for the CT-scan is follow-up of urinary stones * Written informed consent;Ankle CT: * * 18 years old * The indication for the CT-scan is suspected orthopaedic abnormalities * Written informed consent
Exclusion criteria
Exclusion criteria: * 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters are normal-dose CT and low-dose CT. The main endpoints are the subjective and objective image quality at different dose reduction levels for both standard and iterative reconstruction. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are coronary calcifications (cardiac CT), pulmonary nodule volume (chest CT) and detectability and size of urinary concrements (abdominal CT). | — |
Countries
Netherlands