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VMAT for Brain Tumor
Study Summary
This trial will use a novel radiotherapy technique, called volumetric modulated arc therapy (VMAT), to treat patients with brain metastases. VMAT allows for delivery of both a standard radiation dose to the whole brain, as well as a higher radiation dose to the brain metastases at the same time. The study will assess the effectiveness of using VMAT in treating brain metastases, and examine its potential side-effects.
- Metastatic Brain Tumors
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Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Is this experiment actively recruiting participants?
"According to the information posted on clinicaltrials.gov, this investigation is not presently seeking candidates. Initially published in 2010 and last updated in 2021, there are still 887 other trials that have open enrollment for volunteers."
What are the minimum qualifications for enrollment in this clinical experiment?
"This clinical trial seeks to recruit 60 individuals whose age is between 18 and 100. All participants must satisfy the following qualifications: they should have a malignancy diagnosed within the past 5 years; 1-10 brain metastases, with the largest's diameter not exceeding 3 cm; KPS score of 70 or higher; no neurologic instability that requires corticosteroids use; disease outside of their cranium adequately managed (estimated life expectancy 6 months); be available for follow up examinations and imaging tests; prior cranial surgery allowed if applicable."
Are participants below the age of fifty-five eligible for this research endeavor?
"Individuals 18 years of age and above, up to a maximum of 100, may be eligible for this clinical study in accordance with the stated inclusion requirements."
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