Patients with clinical indications for a MRI exam.
Conditions
Interventions
Group 1: MRI examination (no contrast agent)
Sponsors
Siemens AG
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with a clinical indication for an MRT examination Patients, who have been adequately informed and have given their written informed consent for participation in the clinical investigation
Exclusion criteria
Exclusion criteria: Patients who are participating in another study that requires Ethics Committee approval. Non-interventional studies are permitted. Patients with one or more of the following: o Claustrophobia o Cardiac arrhythmia o Cardiac pacemaker o Intrauterine device o Pregnant female patients, and female patients with suspicion of pregnancy o Metal or metal implant in patient´s body o Persons with spasm or seizure disorder o Persons, who are either not adult, not sui juris, or who are institutionalized by court order.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective is to evaluate and further optimize image quality, image resolution and acquisition speed of an innovative MRI system | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary objectives are to evaluate clinical workflow, system handling and patient comfort. These will be evaluated by the investigators for every examination, using a visual analog scale. | — |
Countries
Germany
Contacts
Public ContactEva-Maria Rueth
Siemens AG
Outcome results
None listed