Capturing Real-World Insights to Improve Prostate Cancer Care
Prostate cancer is one of the most common malignancies in men, yet clinical trial populations often don't reflect real-world complexity.
ProReg fills this gap by systematically capturing data on diagnosis, treatment, and outcomes from routine clinical practice.
The registry emphasises what matters to patients—including quality of life, functional outcomes, and symptom burden.
(Patient-Reported Outcome Measures)
Use PROMs to better understand treatment impact from the patient's perspective.
Provide real-world evidence to inform and refine EAU Guidelines.
Allow centres to compare their outcomes with anonymized, aggregate data from across Europe.
Enable data-driven studies on treatment effectiveness, health equity, and long-term outcomes.
State-of-the-art data security with full compliance to European data protection regulations.
Interactive data visualisation tools for immediate insights and trend analysis.
Opportunities for multicentre studies and collaborative research initiatives.
Feedback reports to support clinical audit and quality improvement initiatives.
Live Analytics
Real-time Insights
Data Security
GDPR Compliant
Collaboration
Multicentre Studies
Quality Audit
Feedback Reports
Ensures your voice is heard in prostate cancer care and contributes to improving treatment for all patients.
Helps future patients benefit from better-informed decisions based on real-world evidence and outcomes.
Confidential and voluntary participation, with full data privacy safeguards and GDPR compliance.
ProReg is currently onboarding centres across Europe. Be part of a movement that redefines how prostate cancer care is measured, delivered, and improved.
Contact: datainnovation@uroweb.org