New MRI technique could sharpen cancer radiation targeting
NCT ID NCT04657042
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing a new imaging method called 4D-MRI that creates 3D movies of the lungs and liver as a person breathes. The goal is to help doctors better track tumor movement during radiation therapy, making treatment more precise. Researchers will test this in healthy volunteers and cancer patients to see if it outperforms current CT scans.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this imaging method could help doctors target tumors more precisely during radiation therapy, potentially improving treatment outcomes.
- What could go wrong
- This is an early-stage imaging study in healthy volunteers and a small number of cancer patients. The technique may not improve treatment planning as hoped.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2020
- Expected to finish
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Dec 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Up to 30 lung cancer patients, 30 liver cancer patients, and 40 healthy human volunteers will receive MRI examinations at the University of Virginia to directly measure respiratory motion in the thorax and abdomen. All subject populations will include roughly equal male and female representations. The subject populations will have minority and ethnic representation typical of the local population area that includes the University of Virginia. No specific racial or ethnic group will be excluded. All subjects must have the ability to understand the requirements of the study and must provide informed consent with a personal signature. No persons from vulnerable populations will be included in this study.
- Ages
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18 to 82 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria:The inclusion criteria for lung and liver cancer patients are: * Patient is 21 or older * Patient has primary or metastatic tumor(s) in the lungs or the liver * Diameter of the tumor(s) is less than 7 cm * Patient will receive radiation therapy (ordered by the treating Radiation Oncologist) as part of their treatment regimen * Patient will undergo a planning CT scan with tumor motion assessment (planning 4D-CT ordered by the treating Radiation Oncologist) as part of their treatment regimen * Patient has signed informed consent and is willing to comply with the 4D-MRI imaging protocol The inclusion criteria for healthy volunteers are: * Subject is 18 or older * Subject has signed informed consent and is willing to comply with the 4D-MRI imaging protocol Exclusion Criteria: * Any condition for which a MRI procedure is contraindicated including presence of metallic material in the body, such as pacemakers, non- MRI compatible surgical clips, shrapnel, etc. * Subjects who have difficulty lying flat on their back for extended periods of time * Patients with any serious/poorly controlled medical or psychological conditions that would complicate protocol compliance * Too large to adequately fit in the magnet bore or RF coils * Claustrophobia * Females who are pregnant or lactating * Presence of active or chronic infection
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Virginia
RECRUITINGCharlottesville, Virginia, 22908, United States
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