New MRI scan could detect liver cancer without a biopsy
NCT ID NCT07368049
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will use a special MRI machine to scan the liver for phosphorus and sodium signals in people with liver cancer and healthy volunteers. The goal is to see if these scans can tell the difference between cancerous and healthy tissue. 100 participants will be enrolled to test this imaging technique.
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 could lead to a new, non-invasive way to detect liver cancer using MRI scans.
- What could go wrong
- This is an early exploratory study with no treatment involved. It may not show clear differences between patients and healthy volunteers.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- 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: * 1\. HCC patient group * Age ≥ 18 years; * With clear consciousness, ability to cooperate, and autonomous behavior; * Voluntary agreement to participate in this clinical trial and signing of the subject's informed consent form; * Patients diagnosed with primary hepatocellular carcinoma by imaging or clinical diagnosis, and who have not received tumor treatment. * 2\. Healthy control group * Age ≥ 18 years; * With clear consciousness, ability to cooperate, and autonomous behavior; * Voluntary agreement to participate in this clinical trial and signing of the subject's informed consent form; * No previous history of liver disease. Exclusion Criteria: * HCC patient group and healthy control group * Patients with claustrophobia. * Subject's body temperature \> 39.5°C on the day of scanning. * Females who plan to be pregnant within 6 months, and pregnant and lactating females. * Patients with other implants, prostheses, foreign bodies, patches, etc. that are not suitable for MRI examination; patients with electronic implants, such as pacemakers, stimulators, insulin pumps, cochlear implants, etc. * Critically ill subjects with various resuscitation devices or those with any emergency medical condition requiring first aid. * Subjects with poor compliance are considered to be excluded by the investigators. * Subjects who are not considered suitable for this trial by the investigators.
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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 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.
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