Overview
The aim of the registry is to gather real-life data to evaluate the clinical performance and safety of medical devices in patients who have been treated with HIFU thank to the Focal One device for their prostate cancer.
Description
It is a prospective and retrospective register.
Eligibility
Inclusion Criteria:
- Being treated for prostate cancer with the Focal One device
- Patient does not object and consent\* to the collection of clinical data in the registry
Exclusion Criteria:
- Patient deprived of liberty following a judicial or administrative decision
- Patient under guardianship or curatorship \* if applicable according to local regulation


