Actively Recruiting

Age: 18Years +
MALE
NCT06866782

European Registry of Next Generation Imaging in Advanced Prostate Cancer

Led by Fundacio Puigvert · Updated on 2025-03-11

600

Participants Needed

24

Research Sites

118 weeks

Total Duration

On this page

Sponsors

F

Fundacio Puigvert

Lead Sponsor

E

European Association of Urology Research Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

European Registry of Next Generation Imaging in Advanced Prostate Cancer

Who Can Participate

Age: 18Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult male patients 18 years or older with no upper age limit
  • Histologically confirmed prostate cancer
  • Patients requiring imaging exploration (conventional, NGI, or combination) at high risk for metastatic deposits at hormone-sensitive stage, either at initial diagnosis or biochemical relapse after local treatment
  • Patients who sign a written informed consent form to participate
Not Eligible

You will not qualify if you...

  • Participation in other studies requiring NGI as a triage test for metastatic assessment
  • Presence of any other clinically significant disease or condition that discourages participation according to the investigator
  • Inability to complete the study

AI-Screening

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Trial Site Locations

Total: 24 locations

1

Universitair Ziekenhuis Leuven

Leuven, Belgium

Not Yet Recruiting

2

Hospital Center University De Lille

Lille, France

Not Yet Recruiting

3

Hospices Civils de Lyon

Lyon, France

Not Yet Recruiting

4

University Hospitals Pitié Salpêtrière

Paris, France

Not Yet Recruiting

5

Bonn University Hospital

Bonn, Germany

Not Yet Recruiting

6

Martini Klinik

Hamburg, Germany

Not Yet Recruiting

7

München LMU L MU-University Clinic

Munich, Germany

Not Yet Recruiting

8

Urologische Klinik München - Planegg

Planegg, Germany

Not Yet Recruiting

9

Universitätsklinik Tübingen

Tübingen, Germany

Not Yet Recruiting

10

IRCCS Universit of Bologna

Bologna, Italy

Not Yet Recruiting

11

Azienda Ospedaliero-Universitaria Careggi

Florence, Italy

Actively Recruiting

12

Azienda Ospedaliero-Universitaria Careggi

Florence, Italy

Not Yet Recruiting

13

IRCCS Ospedale San Raffaele

Milan, Italy

Not Yet Recruiting

14

ERASMUS MC & Franciscus Hospital

Rotterdam, Netherlands

Not Yet Recruiting

15

Uniwersytet Jagielloński Collegium Medicum

Krakow, Poland

Not Yet Recruiting

16

Fundació Puigvert

Barcelona, Spain

Actively Recruiting

17

Hospital de la Santa Creu i Sant Pau

Barcelona, Spain

Actively Recruiting

18

Hospital Universitario Reina Sofia

Córdoba, Spain

Not Yet Recruiting

19

Hospital Universitario La Paz

Madrid, Spain

Not Yet Recruiting

20

Hospital Universitario Ramón y Cajal

Madrid, Spain

Not Yet Recruiting

21

Hospital Universitario de Canarias

San Cristóbal de La Laguna, Spain

Actively Recruiting

22

Hospital Universitario Marqués de Valdecilla

Santander, Spain

Not Yet Recruiting

23

Hospital Clínico Universitario de Santiago

Santiago de Compostela, Spain

Not Yet Recruiting

24

Skånes universitetssjukhus Malmö

Malmö, Sweden

Not Yet Recruiting

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Research Team

F

Francesco Sanguedolce, MD, PhD

CONTACT

D

Daria Chernysheva, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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