healthy participants
Conditions
Interventions
Group 1: After informed consent for the planed MRI examination, CIs will be fixed behind the ear of our study subjects. Every subject will first be imaged in a 1.5T MRI with standard sequences and wit
Sponsors
Klinikum der Universität München, Campus Großhadern
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: informed consent, orally and written for MRI age above 18
Exclusion criteria
Exclusion criteria: no informed consent given General exclusion criteria for MRI, like MR-incompatible ferromagnetic implants or pacemakers, pregnancy claustrophobia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of artifact size | — |
Secondary
| Measure | Time frame |
|---|---|
| risk reduction, improved detection of anatomical structures, reduced image distortion, improved subjective imaging quality | — |
Countries
Germany
Contacts
Public ContactChristel Besseler
Klinik und Poliklinik für Radiologie Klinikum der Universität München Campus Großhadern
Outcome results
None listed