NCT03232463
Study for the Evaluation of the Feasibility of Applying Advanced MRI Scanning in Clinical Practice
Enrolling by Invitation
Not specifiedAges 18–65ObservationalNeurological Associates of West Los AngelesInvestigator-initiated
~2,000 participants
Updated 2023-03-24 on ClinicalTrials.gov
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of subjects who successfully complete an fMRI scan
Measured over Through study completion, an average of 1 year
Conditions
Where it's being run
1 sites across 1 statesCalifornia1
Study leadership
- Sheldon Jordan, MD · PRINCIPAL_INVESTIGATOR · Neurological Associates of West Los Angeles
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
The subject is between the ages of 18-65 years old.
The subject clinically needs an advanced MRI
The subject has consented for his/her self.
The subject is fluent in the English language.
The subject is proficient in comprehending verbal and written English.
Exclusion
Aneurism clips
Cardiac pacemaker
Implanted cardioinverter defibrillator
Electronic implant or device
Magnetically activated implant or device
Neurostimulation system
Spinal cord stimulator
Internal electrodes or wires
Bone growth/bone fusion stimulator
Cochlear, otologic, or other ear implant
Insulin or other infusion pump
Implanted drug infusion device
Any type of prosthesis (eye, penile, etc.)
Heart valve prosthesis
Eyelid spring or wire
Artificial or prosthetic limb
No Metallic stent, filter, or coil
Shunt (spinal or intraventricular)
Vascular access port and/or catheter
Radiation seeds or implants
Swan-Ganz or thermodilution catheter
Medication patch (Nicotine, Nitroglycerine)
Any metallic fragment or foreign body
Wire mesh implant
Tissue expander (e.g., breast)
Surgical staples, clips, or metallic sutures
Joint replacement (hip, knee, etc.)
Bone/joint pin, screw, nail, wire, plate, etc.
IUD, diaphragm, or pessary
Dentures or partial plates
Tattoo or permanent makeup
Body piercing jewelry
Hearing aid
Breathing problem or motion disorder
Severe claustrophobia
Prisoners
Minors
Poor/uninsured
Institutionalized
Limited or non-readers
Non-English speaking subjects
Wards of the state
Pregnant women
Nursing home residents recruited in the nursing home
Students of PI or study staff
Students recruited in the educational setting (school, class, etc)
Employees directly supervised by the PI or sub-investigator
Employees of research site or sponsor
Military personnel recruited by military personnel
Cognitively impaired
Adult subjects that cannot consent for themselves
What this trial measures
- Number of subjects who successfully complete an fMRI scanThrough study completion, an average of 1 year
In order to assess scan feasibility, we will keep track of the total number of patients who sign the consent form and are able to complete the fMRI scan.