Status:
COMPLETED
Evaluation of Human Brain Tumor Therapy Response by Magnetic Resonance (MR)
Lead Sponsor:
University of Michigan
Collaborating Sponsors:
National Institutes of Health (NIH)
National Cancer Institute (NCI)
Conditions:
Brain Tumors
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to determine if new MRI methods that measure various information and chemical makeup in the brain, will give early information regarding response to treatment in patients ...
Detailed Description
The purpose of this study is to see if new MRI methods which measure information related to water, blood flow, and chemical makeup in the brain, can give early information of how well treatment is wor...
Eligibility Criteria
Inclusion
- Patients over the age of 18 who have been diagnosed with a brain tumor of the central nervous system and a treatment plan has been discussed.
- Must be willing/able to undergo 3-5 MRI scans with IV contrast.
- You can take part in this study if you are NOT afraid of small, enclosed places.
Exclusion
- A patient who is claustrophobic.
- Females who are pregnant or lactating.
- Patients who have electrically, magnetically or mechanically activated implants such as heart pacemaker, magnetic surgical clips, prosthesis or or implanted neurological stimulator.
- Any patient who has a history of allergic reactions to MR contrast agent (Omniscan, Magnevist, MultiHance)
- Patients who require general anesthesia to complete MRI exam or patients who have had a negative reaction to MRI sedation. (Chloral Hydrate, Pentobarbital or Versed)
- You should NOT have any metals, or implanted devices in your body (such as aneurysm clips, pacemakers, or artificial joints or limbs.). You will need to tell us about your medical history including any surgeries you have had.
- Also, if your job or any other experience might have left metal fragments in your body, please let us know, as the MRI has a strong magnetic field could move a metal fragment in your body or interfere with an implanted device, such as a pacemaker, causing you harm.
Key Trial Info
Start Date :
September 1 1999
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 15 2014
Estimated Enrollment :
88 Patients enrolled
Trial Details
Trial ID
NCT00724191
Start Date
September 1 1999
End Date
January 15 2014
Last Update
May 11 2020
Active Locations (1)
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1
Univeristy of Michigan Health System
Ann Arbor, Michigan, United States, 48109