Condition: Prostate Cancer · Sponsor: Turku University Hospital
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.
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.
| Central Finland Central Hospital | Jyväskylä, Finland | Recruiting |
| Satakunta Central Hospital | Pori, Finland | Recruiting |
| Tampere University Hospital | Tampere, Finland | Recruiting |
| Turku University Hospital | Turku, Finland | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04287088