Comparing Micro-ultrasound and MRI for Prostate Cancer Screening

This study is comparing two imaging methods, microUltrasound (ExactVu) and standard prostate mpMRI, to see which is better at finding important prostate cancers. You might be able to join if you are a man between 50 and 70 years old, have a PSA (Prostate Specific Antigen, a blood test for prostate health) between 3-20, and/or an abnormal DRE (Digital Rectal Exam). You also shouldn't have had a prostate biopsy before. The study aims to find the most effective way to image the prostate to help decide if a biopsy is needed. Participants will be randomly assigned to receive either ExactVu or mpMRI.

Study design
This interventional study plans to enroll 1284 men. Participants will be randomly assigned to one of two groups to compare imaging results.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
After your imaging test, you will be followed for one year to see if clinically significant prostate cancer is detected.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06626022

Screening for Prostate Cancer Using High Resolution Micro-ultrasound Versus Multiparametric Magnetic Resonance Imaging.

Recruiting
PHASE3Ages 50–70InterventionalScreening
University of Alberta
~1,284 participants
Updated 2026-06-04 on ClinicalTrials.gov
What's tested:MRIExactVu

At a glance

Recruiting sites
4 of 9 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Detection of Clinically significant prostate cancer.
Measured over Once enrolled, men will be followed for 1 year after the imaging test.
Prostate Cancer Screening
9 sites across 9 states
California1
Texas1
Alberta1
British Columbia1
Ontario1
Quebec1
France1
Norway1
  • Adam Kinnaird, MD, PhD · PRINCIPAL_INVESTIGATOR · University of Alberta

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  • Detection of Clinically significant prostate cancer.Once enrolled, men will be followed for 1 year after the imaging test.

    The primary objective of this trial is to determine if a screening pathway using microUS is non-inferior to a pathway using MRI for the detection of clinically significant prostate cancer, defined as Gleason Grade Group 2 or more.