New 3D ultrasound could rival MRI for breast cancer screening
NCT ID NCT07216274
First seen Jun 25, 2026 · Last updated Aug 21, 2026 · Updated 4 times
Summary
This study tested a new 3D ultrasound called quantitative transmission imaging (QTI) against standard MRI for breast cancer screening in 26 women at high risk. The goal was to see if QTI could effectively detect suspicious findings. If it works, QTI might offer a faster, less expensive screening option.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- QT Ultrasound Breast Scanner (3D ultrasound)
- What this could lead to
- If successful, this could offer a more accessible, less expensive screening option for women at high risk of breast cancer.
- What could go wrong
- This is a very small, early feasibility study with only 26 participants. The new ultrasound may not be as accurate as MRI, and results may not apply to all women.
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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26 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Oct 2025
- 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 years and older
- Sex
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Female participants only
- 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: * Women 18+ years of age * High lifetime risk of breast cancer as determined by a risk assessment tool such a Tyrer-Cuzick model * Clinical ordered screening MRI. * MRI and QTI performed within 30 days of each other * Breasts that will fit in the quantitate transmission (QT) Ultrasound Breast Scanner (e.g. bra cup size less than DDD) Exclusion Criteria: * Pregnant patients * Lactating patients * Patients with open wounds or discharge * Patients \< 18 years of age * Patients who are \> 350 lbs * Patients who are unable to lay prone for \>15 minutes
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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
-
Mayo Clinic in Rochester
Rochester, Minnesota, 55905, United States
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