Optimisation of Image Quality, Image Resolution and Acquisition SpeedWith an Innovative MRI System
Not Applicable
- Conditions
- Patients with clinical indications for a MRI exam.
- Registration Number
- DRKS00003556
- Lead Sponsor
- Siemens AG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 106
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
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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective is to evaluate and further optimize image quality, image resolution and<br>acquisition speed of an innovative MRI system
- Secondary Outcome Measures
Name Time Method The secondary objectives are to evaluate clinical workflow, system handling and patient<br>comfort. These will be evaluated by the investigators for every examination, using a visual analog scale.