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NCT07416812Completed

Targeted Prostate Cancer Screening in Men With BRCA1/2 Mutations

The Identification of Men With a Genteic Predisposition to Prostate Cancer: Targeted Screening in Men at Higer Genetic Risk and Controls Study

Source: ClinicalTrials.gov · Last updated 18 Feb 2026

Brief summary (registry, in English)

This interventional study is a follow-up component of the IMPACT project, which aims to identify men at increased hereditary risk of prostate cancer. The study focuses on men carrying BRCA1 and BRCA2 germline mutations and a control group of non-carriers. Participants are contacted by telephone to determine whether they developed prostate cancer during 2025 and to collect updated personal and family medical history information. The goal of the study is to support targeted prostate cancer screening programs in men at higher genetic risk.

Status (registry)
Completed
Study type
Interventional
Enrollment
25 (actual)
First submitted
6 Feb 2026
Start date
29 Mar 2021
Primary completion date
30 Nov 2021
Lead sponsor
Institute of Oncology Ljubljana
NCT number
NCT07416812

What you commit to

  • Study type: Interventional
  • Participants enrolled: 25
  • From 29 Mar 2021 to the primary completion date, 30 Nov 2021
  • 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

  • History of prostate cancer prior to enrollment

Other illness

  • Any condition that, in the investigator's opinion, would interfere with study participation or data quality

Other

  • Inability to provide informed consent or complete follow-up procedures

Who the study is looking for

  • Male participants aged 18 years or older
  • BRCA1 or BRCA2 mutation carriers or non-carrier controls enrolled in the IMPACT study
  • Eligible for targeted prostate cancer screening and follow-up
  • Ability to participate in telephone follow-up interview
  • Written informed consent provided

Age in the registry: 18 years to - · Sex: Male · Accepts 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
Institute of Oncology Ljubljana
Coordinator of this site? Confirm its status
LjubljanaSloveniaUnknown status

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