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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 weeks3 visits
Treatment ~ Varies
Follow Up ~ every 3 years up to 15 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~every 3 years up to 15 years
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
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have not had surgery or ablation for my prostate.I have had a hip replacement surgery.I have never been diagnosed with prostate cancer.I do not have a rectum.I am a man aged 18 or older.
Research Study Groups:
This trial has the following groups:- Group 1: High Risk- Positive Germline Mutation (n=40):
- Group 2: High Risk- Family History (n=45):
- Group 3: High Risk- High GRS (n=40):
- Group 4: Low Risk (n=125):
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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