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 with known or suspected prostate cancer who have been referred for a prostate MRI scan, to be followed by a type of biopsy that uses MRI imaging as a guide.
- People who are willing and able to give written consent to take part before the MRI scan takes place.
Who may not be able to join:
- People who are not able to give written consent for themselves.
- People who are unable to follow the study procedures for any reason, or who are unable to communicate with the research team.
- People whose psychiatric condition affects their ability to make their own decision about consenting to take part (note: this applies only where the ability to consent is affected, not to all people with a psychiatric condition).
- People who are currently in prison.
- People under the age of 18.
- People who have already received treatment for prostate cancer, such as surgery, radiation therapy, targeted ablation, hormone therapy, or other chemotherapy.
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: Aytekin Oto, MD, University of Chicago Medicine Comprehensive Cancer Center
Phone: 773-702-8553
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
Decision Map Tool Compared to Oncologists
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.