Protocol Details
Functional and Metabolic Imaging Using Magnetic Resonance at 3.0 Tesla
This study is currently recruiting participants.
Summary | Eligibility | Citations | Contacts
Summary
Number |
99-CC-0163 |
Sponsoring Institute |
National Institutes of Health Clinical Center (CC) |
Recruitment Detail |
Type: Participants currently recruited/enrolled |
Referral Letter Required |
No |
Population Exclusion(s) |
Children |
Special Instructions |
Currently Not Provided |
Keywords |
MRI/MRS; |
Recruitment Keyword(s) |
Healthy Volunteer |
Condition(s) |
Healthy |
Investigational Drug(s) |
None |
Investigational Device(s) |
None |
Intervention(s) |
None |
Supporting Site |
|
Healthy normal volunteers will undergo MRI scanning. For this procedure, the person lies on a stretcher that is moved into a MRI machine, which produces a strong magnetic field. A special lightweight coil is placed on the person's head to obtain better pictures. The scan time ranges from 20 minutes to 2 hours, with the average scan lasting between 45 and 90 minutes.
During the MRI, the person may be asked to perform simple tasks, such as listening to tones or watching a screen, tapping fingers or moving a hand. More complex tasks may require thinking about tones or pictures and responding to them by pressing buttons.
The images produced in this study will be compared with those produced using standard MRI. The results will be used to develop improved imaging methods for better patient care and research.
Eligibility
INCLUSION CRITERIA:
a. age 18 and older
b. capable of providing own informed consent
c. capable of filling out MRI screening form
EXCLUSION CRITERIA:
a. contraindications for MRI including aneurysm clip; implanted neural stimulator; implanted cardiac pacemaker or auto-defibrillator; cochlear implant; ocular foreign body (e.g. metal shavings); or insulin pump, or other metal in the body.
b. pregnancy
c. Subjects will be excluded if it is deemed that they have a condition that would preclude their participation for technical development (e.g. claustrophobia)
d. Subjects will be excluded if they present unnecessary risk (e.g. Brain surgery of uncertain type, etc.).
Citations:
Contacts:
Principal Investigator |
Referral Contact |
For more information: |
| Joseph A. Frank, M.D. National Institutes of Health Clinical Center (CC) National Institutes of Health Building 10 Room B1N256 10 Center Drive Bethesda, Maryland 20892 (301) 402-3586 jafrank@helix.nih.gov |
Bobbi K. Lewis National Institutes of Health Clinical Center (CC) National Institutes of Health Building 10 Room B1N256 10 Center Drive Bethesda, Maryland 20892 (301) 435-3866 blewis@cc.nih.gov |
Patient Recruitment and Public Liaison Office Building 61 10 Cloister Court Bethesda, Maryland 20892-4754 Toll Free: 1-800-411-1222 TTY: 301-594-9774 (local),1-866-411-1010 (toll free) Fax: 301-480-9793 prpl@mail.cc.nih.gov |
Clinical Trials Number:
NCT00001844
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