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Clinical Trials in Poland / NCT06866782
Recruiting Observational

European Registry of Next Generation Imaging in Advanced Prostate Cancer

NCT06866782 · tracked via the Priya Life Science Poland tracker
Phase
Observational
Started
2024-09-17
Last updated
2025-03-11

Condition(s) studied

Prostate CancerAdvanced Prostate CancerMetastatic Prostate Cancer (mPC)

Investigational drug(s) / intervention(s)

Imaging

Imaging: Imaging will be done according to local protocols and/or guidelines of EAU

Study summary

The RING study is a European registry collecting real-world data on advanced prostate cancer (APC) imaging. It aims to evaluate the role of next-generation imaging (NGI), such as PET/CT and whole-body MRI, in detecting and monitoring the disease compared to conventional imaging.

Men aged 18 or older with histologically confirmed prostate cancer are eligible to participate in the study if they require imaging to assess potential metastases, either at diagnosis or after relapse and sign a consent form.

Patients will receive standard care with no experimental treatments. Imaging and treatment decisions will follow routine clinical practice. Data will be collected from medical records and analysed for research. This study will help doctors understand when NGI should be used, how it affects treatment decisions, and its impact on patient outcomes.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Adult male patients (≥18 years with no upper age limit). 2. Histologically proven prostate cancer. 3. Patients who require imaging exploration (conventional, Next-Generation Imaging (NGI), or their combination) at high risk for harbouring metastatic deposits at the hormone-sensitive stage, either at the diagnostic workout of a "naïve" patient or at biochemical relapse/progression after local treatment. 4. Patients who authorize their participation in the study by signing a written informed consent form (ICF). Exclusion Criteria: 1. Patients participating in other interventional or non-interventional study which requires NGI as a triage test for metastatic assessment. 2. Patients with evidence of any other clinically significant disease or condition which in the opinion of the investigator discourages their participation in the study. 3. Patients who will not be able to complete the study.

Primary outcome measure(s)

Trial sites (24)

FacilityCityRegionStatus
Universitair Ziekenhuis Leuven Leuven Belgium Not Yet Recruiting
Hospital Center University De Lille Lille France Not Yet Recruiting
Hospices Civils de Lyon Lyon France Not Yet Recruiting
University Hospitals Pitié Salpêtrière Paris France Not Yet Recruiting
Bonn University Hospital Bonn Germany Not Yet Recruiting
Martini Klinik Hamburg Germany Not Yet Recruiting
München LMU L MU-University Clinic Munich Germany Not Yet Recruiting
Urologische Klinik München - Planegg Planegg Germany Not Yet Recruiting
Universitätsklinik Tübingen Tübingen Germany Not Yet Recruiting
IRCCS Universit of Bologna Bologna Italy Not Yet Recruiting
Azienda Ospedaliero-Universitaria Careggi Florence Italy Recruiting
Azienda Ospedaliero-Universitaria Careggi Florence Italy Not Yet Recruiting
IRCCS Ospedale San Raffaele Milan Italy Not Yet Recruiting
ERASMUS MC & Franciscus Hospital Rotterdam Netherlands Not Yet Recruiting
Uniwersytet Jagielloński Collegium Medicum Krakow Poland Not Yet Recruiting
Fundació Puigvert Barcelona Spain Recruiting
Hospital de la Santa Creu i Sant Pau Barcelona Spain Recruiting
Hospital Universitario Reina Sofia Córdoba Spain Not Yet Recruiting
Hospital Universitario La Paz Madrid Spain Not Yet Recruiting
Hospital Universitario Ramón y Cajal Madrid Spain Not Yet Recruiting
Hospital Universitario de Canarias San Cristóbal de La Laguna Spain Recruiting
Hospital Universitario Marqués de Valdecilla Santander Spain Not Yet Recruiting
Hospital Clínico Universitario de Santiago Santiago de Compostela Spain Not Yet Recruiting
Skånes universitetssjukhus Malmö Malmö Sweden Not Yet Recruiting

Other trials for the same condition

Official registry record

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.

View NCT06866782 on ClinicalTrials.gov ↗ ← All trials in Poland