The study examines without organ restriction whether the implementation of accelerated or improved MRI sequences in clinical routine is feasible, and what information these new sequences have in comparison to routine sequences.
Conditions
Interventions
Group 1: Patients who receive a diagnostic MRI scan at the Department of Diagnostic and Interventional Radiology at the University Hospital Freiburg.
Sponsors
Klinik für Diagnostische und Interventionelle Radiologie Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Diagnostic MRI examination at the Department of Diagnostic and Interventional Radiology of the University Hospital Freiburg
Exclusion criteria
Exclusion criteria: General exclusion criteria for MRI scans: metal implants that are not suitable for MRI, other implants that are not suitable for MRI, allergic reaction towards MRI contrast agent (given the accelerated/optimized sequence is contrast agent dependent), patients <18years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intra-individual comparison of image quality between accelerated/optimized MRI sequences with routine sequences. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the diagnostic accuracy of the accelerated/optimized sequences with regard to the individual clinical question compared with routine sequences. | — |
Countries
Germany
Contacts
Public ContactMatthias Benndorf
Klinik für Diagnostische und Interventionelle Radiologie, Universitätsklinikum Freiburg
Outcome results
None listed