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Imaging

MRI Screening for Prostate Cancer

N/A
Recruiting
Led By Scott Eggener, MD
Research Sponsored by University of Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up every 3 years up to 15 years
Awards & highlights
No Placebo-Only Group

Summary

This trial will test if MRI can spot prostate cancer earlier in high-risk men.

Who is the study for?
This trial is for men aged 18 and older who are at high risk of developing prostate cancer but have no known history of it. They should not have had any previous prostate surgery or a biopsy within the last three years, nor an MRI in that time frame. Men with metal fragments, severe claustrophobia, without a rectum, or those who've had hip replacement are excluded.
What is being tested?
The study is testing if using Magnetic Resonance Imaging (MRI) can detect serious types of prostate cancer earlier and more reliably in men considered to be at high risk for this disease.
What are the potential side effects?
Since the intervention involves MRI screening, there may be discomfort due to lying still during the procedure. There's also a small chance of an allergic reaction to contrast materials if used. Claustrophobic individuals might experience anxiety.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~every 3 years up to 15 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and every 3 years up to 15 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Malignant Neoplasms

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

4Treatment groups
Experimental Treatment
Group I: Low Risk (n=125):Experimental Treatment1 Intervention
No known germline mutation, low genetic risk score (GRS \<1.5), and no known family history of prostate cancer.
Group II: High Risk- Positive Germline Mutation (n=40):Experimental Treatment1 Intervention
Men who harbor known germline mutations that have been associated with an increased risk of prostate cancer and aggressive disease (e.g. BRCA2, ATM, PALB2, etc.) with or without a known family history of prostate cancer.
Group III: High Risk- High GRS (n=40):Experimental Treatment1 Intervention
Men who harbor significantly increased disease risk based upon genetic risk score (GRS) value \>1.5 with or without a known family history of prostate cancer.
Group IV: High Risk- Family History (n=45):Experimental Treatment1 Intervention
Men with a family history of prostate cancer in at least one sibling, father, uncle, or grandfather but no known increased genetic risk of prostate cancer (has no pathogenic or likely pathogenic mutation along with a low genetic risk score (GRS\<1.5).

Find a Location

Who is running the clinical trial?

University of ChicagoLead Sponsor
1,053 Previous Clinical Trials
758,824 Total Patients Enrolled
Scott Eggener, MDPrincipal InvestigatorUniversity of Chicago
5 Previous Clinical Trials
660 Total Patients Enrolled

Media Library

Prostate MRI (Imaging) Clinical Trial Eligibility Overview. Trial Name: NCT05608694 — N/A
Prostate Cancer Screening Research Study Groups: High Risk- Positive Germline Mutation (n=40):, High Risk- Family History (n=45):, High Risk- High GRS (n=40):, Low Risk (n=125):
Prostate Cancer Screening Clinical Trial 2023: Prostate MRI Highlights & Side Effects. Trial Name: NCT05608694 — N/A
Prostate MRI (Imaging) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05608694 — N/A
~167 spots leftby Mar 2037