New MRI techniques could sharpen breast cancer detection
NCT ID NCT07608081
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to see if new, advanced MRI scans can more accurately diagnose breast cancer and measure how well treatment is working. Researchers will enroll 1000 women with suspicious breast lumps. The goal is to help doctors create more personalized treatment plans and improve patient outcomes.
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 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Oct 2027
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.
- Ages
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18 to 80 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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. Age ≥ 18 years old 2. Female patients with BI-RADS class 4 or above breast lesions detected by mammography or ultrasound 3. Perform breast new technology MRI examination (ultra fast DCE-MRI、OGSE 、MRE、vMRE)within one week before biopsy or surgery Exclusion Criteria: 1. Previously received breast radiotherapy, chemotherapy, surgery, or targeted therapy 2. Unable to cooperate in completing MRI examination 3. The image data contains serious artifacts (such as motion artifacts and metal artifacts), making it impossible to measure parameters 4. The lesion cannot be clearly identified and outlined on the image 5. Pregnant and lactating women 6. Combined with severe liver, liver, and kidney diseases, coagulation dysfunction, or other malignant tumors
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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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Yunnan Cancer Hospital
RECRUITINGKunming, Yunnan, 650118, China
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