Refinement and Assessment of New Magnetic Resonance Imaging Technologies for Neurological Exams
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|ClinicalTrials.gov Identifier: NCT00739518|
Recruitment Status : Enrolling by invitation
First Posted : August 21, 2008
Last Update Posted : April 26, 2019
|Condition or disease||Intervention/treatment||Phase|
|Nervous System Diseases||Procedure: MRI||Not Applicable|
This study is being done to assess new Magnetic Resonance Imaging (MRI) technologies such as new hardware or software designed to improve MRI examinations of the brain, spine, and head & neck regions.
Software and hardware are constantly being improved, new machines replace old machines, software is updated and improved as are the devices used to produce better MRI images.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||500 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Refinement and Assessment of New Magnetic Resonance Imaging (MRI) Technologies|
|Study Start Date :||October 2004|
|Estimated Primary Completion Date :||January 2021|
|Estimated Study Completion Date :||January 2021|
Experimental: MRI scan - new technology
The patient's clinical MRI scan will also utilize some new technology, such as a change in software or additional MRI sequences
Neurological MRI with new technology evaluation. The new technology may involve software or MRI scanning sequences. This is a long term research study that focuses on new technology that is constantly being created.
- Improvement in quality of MRI studies in Neuroradiology [ Time Frame: 1 year ]
Specific Measurement Are:
- Scan speed - is the new method as fast or faster than regular method(s)
- Signal to noise - Subjectively, or quantitatively do we get the same, better, or new contrast compared to the regular methods(s).
- Image contrast - Subjectively, or quantitatively do we get the same or better resolution compared to the regular method(s).
- Spatial resolution - Subjectively, or quantitatively do we get the same or better resolution compared to the regular method(s).
- Artifact - Subjectively, or quantitatively do we get the better artifact reduction compared to the regular method(s).
- Ergonomics - Is the new software easier to work or offer more information more cleanly than the regular software
- Patient comfort - Subjectively, does the new software and/or hardware make the patient's MRI experience more comfortable.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00739518
|United States, Michigan|
|University of Michigan Health System|
|Ann Arbor, Michigan, United States, 48109|
|Principal Investigator:||Ashok Srivinasan, MD||University of Michigan|