New MRI trick could spot breast cancer without extra gadgets
NCT ID NCT07608068
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new MRI technique called virtual MR elastography (vMRE) that uses standard scans to measure breast tissue stiffness, which can help tell benign from malignant lesions. Researchers will compare vMRE to the traditional MRE method in 238 women with suspicious breast findings. The goal is to see if vMRE can replace or supplement MRE, making diagnosis easier and more widely available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual MR Elastography (vMRE) via diffusion-weighted MRI
- What this could lead to
- If successful, vMRE could provide a simpler, more accessible way to diagnose breast cancer using standard MRI, reducing the need for specialized scans.
- What could go wrong
- This is an early-stage diagnostic study, not a treatment trial. The new technique may not be as accurate as standard MRE, and results may not apply to all patients or settings.
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
-
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 238 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Oct 2025
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
-
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.
- Ages
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18 to 80 years
- Sex
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Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 18 years or older * Female patients with breast lesions BI-RADS category 4 and above on mammography or ultrasound * Breast MRE and vMRE examinations should be performed within 2 weeks prior to needle biopsy or surgery * Obtaining definitive pathology via needle biopsy or postoperatively Exclusion Criteria: * Pregnant and lactating women * Previous history of breast treatment (e.g., surgery, radiotherapy, chemotherapy, or targeted therapy, etc.) * Inability to cooperate for MRI examination, or presence of severe artifacts (e.g., motion artifacts, metal artifacts) in the imaging data that precludes parameter measurement. * The lesion cannot be clearly identified or delineated on MRE or vMRE images * Complicated by severe cardiac, hepatic, or renal diseases, coagulation disorders, or other malignancies.
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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.
Contacts and locations
Locations
-
Yunnan Cancer Hospital
Kunming, Yunnan, China
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