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Study identifier: NCT04287088 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

bpMRI and Risk Based Shared Clinical Decision Making in Prostate Cancer Diagnosis

Condition: Prostate Cancer  ·  Sponsor: Turku University Hospital

PhaseNA
Planned participants600
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The shortcoming of the pre-biopsy prostate MRI approach is the recommendation to biopsy all men post-MRI even if there is no lesion seen in MRI, ie. risk of PCa is very low. Therefore, the primary objective of this trial is to compare if there is a difference between significant cancer detection rate in men undergoing prostate biopsies after MRI scan compared to men undergoing post-MRI prostate biopsies only after a shared decision-making based on prostate cancer risk estimation. The trial will enrol 600 patients. The primary outcome measure is the the proportion of men with CSPCa (Gleason 4+3 prostate cancer or higher) between the control and intervention arms at baseline. Eligible men are randomised 1:1 in two groups. In control arm in all men prostate biopsies are performed after MRI whereas in intervention arm prostate biopsies are performed only after a shared decision-making between urologist and the patient and the discussion is based on risk estimation.

This description comes directly from the study's public registry record.

Talk to the study team

Peter Boström, MD  ·  023130000  ·  peter.bostrom@tyks.fi

Otto Ettala, MD  ·  023130000  ·  otto.ettala@tyks.fi

Always discuss trial participation with your own doctor first.

Locations (4)

Central Finland Central HospitalJyväskylä, FinlandRecruiting
Satakunta Central HospitalPori, FinlandRecruiting
Tampere University HospitalTampere, FinlandRecruiting
Turku University HospitalTurku, FinlandRecruiting

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Source record: clinicaltrials.gov/study/NCT04287088