Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

John Graff, PhD 7346654108
john.graff@arborresearch.org


Naveen Fawas, BS 7346654108
naveen.fawaz@arborresearch.org


Study Location:

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Be Part of Research - Trial Details - Pancreatic Cancer Early Detection Consortium

Pancreatic Cancer Early Detection Consortium

Recruiting

Open to: ALL

Age: 18.0 - 90.0

Medical Conditions

Pancreatic Neoplasms
Pancreatic Cyst
Genetic Predisposition to Disease


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The purpose of the Pancreatic Cancer Early Detection (PRECEDE) Consortium is to conduct research on multiple aspects of early detection and prevention of pancreatic ductal adenocarcinoma (PDAC) by establishing a multisite cohort of individuals with family history of PDAC and/or individuals carrying pathogenic/likely pathogenic germline variants (PGVs) in genes linked to PDAC risk for longitudinal follow up.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Sep 2020 Dec 2030

OBSERVATIONAL



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • University of Liverpool
    Liverpool


The study is sponsored by Arbor Research Collaborative for Health




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Read full details for Trial ID: NCT04970056
Last updated 06 March 2025

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.