Prostate Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 18 years of age or older at the time of the examination
- People who have given their written agreement (informed consent) to take part
- People who have one or more areas of concern found on a prostate MRI scan, rated on a standard scoring system (PI-RADSv2.1) with a score of 1 or higher, at the IRCCS Azienda Ospedaliero-Universitaria hospital in Bologna
- People for whom doctors at the IRCCS Azienda Ospedaliero-Universitaria hospital in Bologna have recommended a specific type of prostate biopsy that combines ultrasound-guided targeting with a broader sampling approach
Who may not be able to join:
- People who have previously had prostate surgery or received hormone therapy for prostate conditions
- People whose scan results are too poor in quality to be used, for example due to interference caused by a hip replacement, movement during the scan, or similar issues
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Caterina Gaudiano, MD, IRCCS Azienda Ospedaliero-Universitaria di Bologna
Phone: +39 0515142307
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Specificity (SP); Sensitivity (SN); Positive Predictive Value (PPV); Negative Predictive Value (NPV)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.