Prospective technical / experimental study
Conditions
Interventions
Group 1: Healthy volunteers:
MRI data is collected from healthy test subjects at one appointment, which is provided with movement artefacts under guidance. This data is used to test and validate new
Sponsors
Klinikum rechts der Isar / TUM
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Healthy, adult volunteers.
Exclusion criteria
Exclusion criteria: a. Refusal of the study by the study participant and lack of capacity to consent. b. Study participants with pronounced claustrophobia. c. Study participants with contraindications for an MRI examination, e.g. pacemaker, implanted defibrillator, artificial heart valves, cardioseal, aneurysm clips that are not MR-compatible, implanted ferromagnetic metal parts (screws, plates from operations), cochlear implants, metal splinters/grenade splinters, acupuncture needles, insulin pump, non-removable piercings. d. Study participants who are or could be pregnant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sharpness, resolution and robustness against motion artifacts | — |
Secondary
| Measure | Time frame |
|---|---|
| Degree of movement which allows a comparable diagnostic image quality compared to images without motion artifacts | — |
Countries
Germany
Contacts
Public ContactStefan Ruschke
Institut fu¨r diagnostische und interventionelle Radiologie, Klinikum rechts der Isar / TUM
Outcome results
None listed