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:

Charles Piercy
charles.piercy@nhs.net


Mr Ben Creagh-Brown
bencb@nhs.net


Study Location:

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Be Part of Research - Trial Details - JEDI-2

JEDI-2

Recruiting

Open to: Female / Male

Age: 18 Years - N/A

Medical Conditions

Other diseases of blood and blood-forming organs


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 immune system is a complex series of cells and molecules that interacts with every tissue and system in the body, including the endothelial cells that line blood vessels. When the body is exposed to infection or trauma, inflammation can start to damage the body. When immune cells damage endothelial cells, changes happen to the instructional molecules (mRNA) which alter function. This change in function allows fluid from your blood can leak into the surrounding tissues, blood pressure drops and blood clotting. This leads to organ damage and death. This study aims to capture endothelial cells from patients exposed to trauma (surgery) or infection (sepsis) with the intention to study the change in mRNA.
During a previous study, our research team tested the feasibility of using a technique known as endovascular biopsy to safely isolate these cells from patients. The procedure involves inserting a cannula into a forearm vein of a patient, then gently passing a small guidewire into the vessel to isolate endothelial cells. These cells are then isolated in a laboratory. For this study we plan to use this technique again to isolate endothelial cells while taking a blood sample at the same time.
All participants involved in this study will be a patient at Royal Surrey Hospital. They will either be undergoing major abdominal surgery and requiring recovery in Intensive Care or admitted to Intensive Care due to severe illness. Patient involvement in the study will last 3 days post enrolment and will not affect any other aspects of their care.

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:

16 Jul 2024 12 Mar 2026

Observational

Observational type: Cohort study;



You can take part if:



You may not be able to take part if:


Healthy volunteer • Not currently a patient within the hospital • Absence of inflammatory diseases and disorders including but not limited to arthritis, peripheral artery disease, vasculitis, diabetes, cardiovascular disease and CKD. • Not on immunomodulatory medications, such as corticosteroids • History of recent major trauma within the last 2 months (e.g., surgery or injury requiring hospitalisation) Surgical patients • Inadequate English language proficiency • Prisoners • Anticipated prohibitively difficult venous cannulation • Presenting with inflammatory diseases and disorders including but not limited to arthritis, peripheral artery disease, vasculitis, sepsis, diabetes with end organ damage, cardiovascular disease and CKD • Currently prescribed immunomodulatory medication or immunocompromised • Received chemotherapy within 2 weeks of predicted sampling • Receiving vasopressor support prior to surgery • History of recent major trauma within the last 2 months (e.g., surgery or injury requiring hospitalisation) Critically ill patients • Inadequate English language proficiency • Prisoners • Anticipated prohibitively difficult venous cannulation • Presenting with inflammatory diseases and disorders including but not limited to arthritis, peripheral artery disease, vasculitis, diabetes with end organ damage, cardiovascular disease and CKD. • Currently prescribed immunomodulatory medication or immunocompromised • Received chemotherapy within 2 weeks of predicted sampling. • History of recent major trauma within the last 2 months (e.g., surgery or injury requiring hospitalisation)


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

  • Royal Surrey County Hospital
    Egerton Road
    Guildford
    Surrey
    GU2 7XX

Charles Piercy
charles.piercy@nhs.net


Mr Ben Creagh-Brown
bencb@nhs.net



The study is sponsored by ROYAL SURREY COUNTY HOSPITAL NHS FOUNDATION TRUST and funded by European Society of Intensive Care Medicine; University of Surrey; GUTS; .




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for Trial ID: CPMS 61240

Last updated 25 April 2025

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