Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06866782

European Registry of Next Generation Imaging in Advanced Prostate Cancer

Status
Recruiting
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
Fundacio Puigvert · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

This registry is intended to collect real-world data on patient demographics, medical history, clinical endpoints, histological tumour characteristics and imaging explorations of the patients with prostate cancer at high risk for harbouring metastatic deposits at the hormone-sensitive stage, who require imaging exploration (conventional, NGI, or their combination) either at the diagnostic workup of a "naïve" patient or at biochemical relapse/progression after local treatment. Stage 1: cross-sectional observation 1. To identify the proportion of patients for whom an imaging work-up with NGI at baseline may result beneficial, according to physician criteria. 2. Assess management prompted by NGI vs. conventional imaging in usual clinical practice. 3. To identify the proportion of patients for whom conventional imaging is considered informative enough for making a clinical decision, according to physician criteria. 4. Stratification of metastatic prostate cancer patients by the number, volume, and location of deposits, according to the different imaging tools employed. 5. Reclassification of HSPC (M0 vs low vs. high volume) based on NGI respect to CI when both imaging modalities are used. Stage 2: longitudinal observation 1\. Evaluation of survival outcomes and their relationship with the imaging pathway undertaken (overall and per subgroup of imaging modality). 2. Identification of prognostic factors related to treatment response and disease progression.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTImagingImaging will be done according to local protocols and/or guidelines of EAU

Timeline

Start date
2024-09-17
Primary completion
2025-12-23
Completion
2026-12-23
First posted
2025-03-10
Last updated
2025-03-11

Locations

24 sites across 8 countries: Belgium, France, Germany, Italy, Netherlands, Poland, Spain, Sweden

Source: ClinicalTrials.gov record NCT06866782. Inclusion in this directory is not an endorsement.