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NCT01990521Active, not recruiting

Prostate Screening Study Using MRI in BRCA Carriers

Screening Male BRCA Mutation Carriers: Effectiveness of Multispectral 3T Magnetic Resonance Imaging

Source: ClinicalTrials.gov · Last updated 9 Sept 2025

Brief summary (registry, in English)

Men with a BRCA1 or BRCA2 mutation are at increased risk for early onset, aggressive prostate cancer compared to men in the general population. Standard of care screening for men with a BRCA mutation includes PSA testing and digital rectal examination (DRE), the same as with men in the general population. This study is being done to assess whether there is value in using MRI as a screening tool to detect prostate cancer at an earlier stage than may otherwise be detected using standard of care screening (PSA, DRE). It is unclear whether MRI has utility as a screening tool in this specific population at high risk for aggressive disease.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
15 Nov 2013
Start date
Jan 2014
Primary completion date
Sept 2025
Lead sponsor
Toronto Sunnybrook Regional Cancer Centre
NCT number
NCT01990521

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From Jan 2014 to the primary completion date, Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindication to receiving low molecular weight MRI contrast agent
  • Previously diagnosed with prostate cancer

Other

  • Claustrophobia
  • Contraindication to MRI

Who the study is looking for

  • Enrolled in the Male Hereditary Cancer Research Program at Sunnybrook Health Sciences Center.
  • Have positive genetic testing for a pathogenic BRCA1 or BRCA2 mutation.
  • Clinically eligible for and willing to undergo ultrasound biopsy within 4 weeks after the MRI.
  • Be 50 years of age or older.

Age in the registry: 50 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sunnybrook Odette Cancer Centre
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.