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.
Eligibility
Sex
MALE
Min age
—
Max age
—
Healthy volunteers
No
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
Primary outcome measure(s)
To monitor the safety of HIFU treatment with the Focal One in patients treated for prostate cancer. — From HIFU treatment up to 5 years post-HIFU Safety will be assessed by collecting adverse events related to HIFU treatment.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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