New ultrasound tech could rival MRI for prostate cancer detection
NCT ID NCT05471128
First seen Jun 25, 2026 · Last updated Aug 19, 2026 · Updated 3 times
Summary
This study compares two methods for detecting serious prostate cancer: MRI fusion biopsy and micro-ultrasound (ExactVu). Researchers want to see if micro-ultrasound can find dangerous cancers as well as MRI, and if it can be used in communities with limited healthcare access. The study involves 29 men scheduled for biopsy.
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 show that micro-ultrasound is a reliable, more accessible alternative to MRI for detecting serious prostate cancer.
- What could go wrong
- This is a small, early-stage study with only 29 participants, so results may not apply to everyone. The technology may not be as accurate 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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29 people
The number who actually took part.
- Started
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Jan 2023
- Expected to finish
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Sep 2026
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
The study population will cover all races, including socioeconomically disadvantaged minorities, that have been diagnosed with prostate cancer.
- Ages
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18 to 99 years
- Sex
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Male participants only
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. Patients scheduled to undergo biopsy and with one of the following: * Men with suspicion of prostate cancer * Men on active surveillance 2. Age ≥18 \[30\] 3. Have available multiparametric prostate MRI 4. Able to provide written, informed consent 5. No significant medical illness which in the opinion of the Investigator would preclude entry to study procedures 6. Be willing and able to comply with scheduled visits Exclusion Criteria: 1. Previously confirmed prostate cancer diagnosis with Grade Group \>= 2 2. Unable to undergo prostate biopsy 3. Prostate MRI unable to be evaluated using the PI-RADS v2 criteria 4. Men with contraindication for MRI or a prostate biopsy 5. Prostate biopsy within 8 weeks prior to mpMRI. 6. Any history of prostate treatment
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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
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University of Oklahoma Health Sciences Center, Stephenson Cancer Center
Oklahoma City, Oklahoma, 73104, United States
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Other studies related to the condition(s) this trial covers.
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