High Resolution Magnetic Resonance Imaging in Patients With Brain Tumors
Status: | Completed |
---|---|
Conditions: | Brain Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 1/3/2019 |
Start Date: | August 28, 2009 |
End Date: | April 20, 2018 |
The study will compare two different size MRI's of a brain tumor.
The study is designed to directly compare the MR images of a brain tumor obtained on the 3T
and then 7T MRI in approximately 150 patients followed serially with MR imaging to evaluate
for tumor progression.
and then 7T MRI in approximately 150 patients followed serially with MR imaging to evaluate
for tumor progression.
Inclusion Criteria:
- Male or female, age 18 years or older
- Patient must meet at least one of the four following criteria regarding brain tumor
diagnosis:
- Histological diagnosis of a brain tumor
- Histological diagnosis of systemic cancer and brain MR imaging suggestive of
metastatic disease to the brain
- Pre-operative brain MR imaging suggestive of a brain tumor
- Radiographic diagnosis of brain tumor in an inoperable location (e.g., brainstem)
- Patient able and willing to provide informed consent
- Karnofsky Performance status > 70%
- Life expectancy greater than 3 months
- Negative serum or urine pregnancy test or child bearing potential terminated by
surgery, radiation, menopause or current use of two approved methods of birth control
- Patients who are excluded from 7T MR imaging because of titanium implants that are not
yet established to be safe at 7T remain eligible for the imaging at 3T * Spanish
speaking participants will be enrolled for this study
Exclusion Criteria:
- Body weight >137 Kg (300 lbs)
- Patient unable to provide informed consent
- Karnofsky Performance status < 70%
- Patients who are claustrophobic or have other contraindications to MRI, such as
implanted pacemaker device vascular clips, surgical clips, prosthetic valves,
pacemakers, otologic implants
- NYHA class III and IV congestive heart failure
- Psychiatric or addictive disorders that preclude obtaining informed consent
- Unstable angina
- Sexually active patients of childbearing potential not using a reliable contraceptive
method
- Pregnant or lactating women
- Women of childbearing potential who refuse a pregnancy test (performed during
screening)
We found this trial at
1
site
2201 Inwood Rd
Dallas, Texas 75235
Dallas, Texas 75235
(214) 645-8300
Principal Investigator: Elizabeth Maher, MD
U.T. Southwestern Medical Center The story of UT Southwestern Medical Center is one of commitment...
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