Study for the Evaluation of the Feasibility of Applying Advanced MRI Scanning in Clinical Practice

Part of paid clinical trials in Santa Monica, California.

Sponsor
Neurological Associates of West Los Angeles
Study ID
NCT03232463
Status
Enrolling By Invitation

Conditions

  • Functional Magnetic Resonance Imaging

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Not accepted

Study Details

The purpose of this research study is to evaluate the feasibility in conducting advanced MRI sequences in a clinical setting. The study will be observational in nature, and will only evaluate the studies of patients that have already been prescribed an advanced MRI for clinical neurological purposes. The only difference for the subject in participating in this study is that the data and information about their scan can be used and disclosed for research purposes, which is understanding if the time of the scan, patient comfort, and quality of the data are feasible. Standard MRI's have been extremely beneficial in the diagnosis and assessment of disease, injury, and anomalies throughout the body. Adding advanced MRI sequences to the arsenal of current standard MRI sequences, as well as analyzing the clinical significance of the data, may improve the benefits of MRI in the future. Within this scope, the study will be looking at the following factors: 1. The total time of the scan, including: * Patient arrival time/lateness * Patient preparation time * Time scanner is being occupied * Patient compliance (is the patient continually stopping the study for breaks, fear, movement, etc) 2. Patient dropout rate, including: * Change of mind * Cost of study is too much * Failure to finish the scan 3. Usability of data, including: * Movement artifact * Patient requiring re-scan for any reason The scan will consist of several advanced MRI sequences that will average between 7-15 minutes each, in addition to a routine 5 minute standard MRI sequence. The variability in the number of advanced sequences depends on the prescription and patient history. All sequences are performed using an FDA-approved MRI scanner.

Key Dates

Start date
Jun 14, 2016
Status verified
Mar 2023
Primary completion
Dec 30, 2025
Completion
Dec 31, 2030

Study Design

Enrollment
2,000 participants (estimated)

Primary Outcome Measure

Number of subjects who successfully complete an fMRI scan [ Time Frame: Through study completion, an average of 1 year ]

Locations (1)

FacilityCityStateZIPSite coordinators
Neurological Associates of West Los AngelesSanta MonicaCalifornia90403-

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