No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins · Other
Who this trial is looking for
This trial is looking for adults with a type of brain cancer called glioblastoma. Participants will undergo a special MRI to help find the best areas for their radiation treatment.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with glioblastoma or grade 4 astrocytoma.
I am over 18 years old.
My KPS score is at least 60.
I have normal organ and blood function.
I understand the study and am willing to sign a consent form.
I can use birth control during the study if I could get pregnant.
You may not be able to join if
I cannot have an MRI.
I am receiving another experimental cancer treatment right now.
I have had prior radiation therapy to the brain.
I have uncontrolled infections or serious health issues.
I am pregnant or breastfeeding.
I cannot use birth control during the study.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This is a research study to determine if a novel molecular magnetic resonance imaging (MRI) technique, called amide proton transfer (APT) imaging, is useful in identifying the most aggressive areas of tumor needed for radiotherapy of brain tumors.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
* Histologic confirmation of glioblastoma or grade 4 astrocytoma
* Age \>18
* KPS at least 60
* Patients must have normal organ and marrow function as defined below:
* leukocytes \>3,000/mcL
* absolute neutrophil count \>1,500/mcL
* platelets \>100,000/mcL
* total bilir…
Inclusion Criteria:
* Histologic confirmation of glioblastoma or grade 4 astrocytoma
* Age \>18
* KPS at least 60
* Patients must have normal organ and marrow function as defined below:
* leukocytes \>3,000/mcL
* absolute neutrophil count \>1,500/mcL
* platelets \>100,000/mcL
* total bilirubin within normal institutional limits
* AST(SGOT)/ALT(SGPT) \<2.5
* institutional upper limit of normal
* creatinine within normal institutional limits OR creatinine clearance \>60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.
* Patients of child-bearing potential (male or female) must practice adequate contraception due to possible harmful effects of radiation therapy on an unborn child.
* Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
* Patients who are unable to receive MRIs will be excluded from the study.
* Patients may not be receiving any other investigational cancer treatment agents at the time of enrollment.
* Patients may not have previously been treated with an overlapping course of radiotherapy to the brain.
* Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
* Pregnant and/or breastfeeding women are excluded. Women of child-bearing potential who are unwilling or unable to use an acceptable method of birth control to avoid pregnancy for the entire study period and up to 12 weeks after the study are excluded. Male subjects must also agree to use effective contraception for the same period as above.
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