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Search / Trial NCT05710380

MRI Risk Maps for Prostate Cancer Diagnosis Using Targeted Biopsy

Launched by UNIVERSITY OF CHICAGO · Jan 25, 2023

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Prostate Cancer

ClinConnect Summary

This clinical trial is investigating a new software developed by researchers at the University of Chicago that helps doctors analyze MRI images of the prostate. The goal is to improve the diagnosis of prostate cancer by using targeted biopsies, which are procedures where small samples of tissue are taken from the prostate to check for cancer. If you are a male between the ages of 65 and 74 and have been referred for an MRI due to suspected prostate cancer, you may be eligible to participate in this study.

Participants will need to undergo one MRI scan and 1-2 biopsies over the course of about 12 months, during which the researchers will monitor your progress. To join the study, you must provide written consent and be able to understand the process. However, individuals who cannot give consent, those with certain psychiatric disorders, prisoners, or minors cannot participate. This trial aims to enhance the way doctors diagnose prostate cancer, ultimately leading to better treatment outcomes for patients.

Gender

MALE

Eligibility criteria

  • Inclusion Criteria:
  • Patients with known or suspected prostate cancer who have been referred for a diagnostic magnetic resonance imaging (MRI) exam of the prostate, to be followed by an MRI-guided fusion biopsy of the prostate.
  • Voluntary written informed consent before the MRI examination.
  • Exclusion Criteria:
  • Subjects incapable of giving informed written consent.
  • Subjects who cannot adhere to the experimental protocols for any reason, or have an inability to communicate with the researcher;
  • Subjects with psychiatric disorders that affect their ability to consent for themselves will be excluded and not the entire population of patients with psychiatric disorders.
  • Prisoners.
  • Minor children (under the age of 18 years old).
  • Patients with previous treatments (surgery, radiation, focal ablation, hormone or other chemotherapy) for prostate cancer.

About University Of Chicago

The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Aytekin Oto, MD

Study Chair

University of Chicago Medicine Comprehensive Cancer Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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