C50
Conditions
Interventions
Group 1: 18 patients with known contrast-enhancing lesions who, in addition to their routine examination, receive an examination for study purposes with a reduced contrast agent dose of 20 % of the st
Sponsors
Universitätsklinikum Aachen
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -Participants gave written informed consent to participate in the study based on thourough oral and written information. -Participants are legally capable and mentally able to follow the instructions of the study personnel.
Exclusion criteria
Exclusion criteria: -If the patients are pregnant or breastfeeding. A missing period in women of childbearing age, which could indicate a possible pregnancy, is considered an exclusion criterion. A pregnancy test will not be carried out. However, there is no health risk to the participant or her child assumed as a result of participating in the study. -If the participant is under guardianship or has been placed in an institution by order of the authorities or court. -If the participant suffers from claustrophobia ("claustrophobia"). -If there is foreign material in/on the body that is unsuitable for MRI. -If lying down for long periods constitutes a burden for the participant, for example due to a back problem.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of the image quality between the artifical intelligence-enhanced low dose examination and the clinical routine examination by two experienced radiologists | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the image quality between both examinations by means of numerical measures that are well established in research on artificial intelligence | — |
Countries
Germany
Contacts
Public ContactChristiane Kuhl
Universitätsklinikum Aachen
Outcome results
None listed