Genomic Determinants of Outcome in Cardiogenic Shock

Recruiting Observational Study
Cardiogenic Shock
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 80
Sex
Any
Study type
Observational
Participants needed
300 (estimated)
Sponsor
Barts & The London NHS Trust · Other
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About This Trial

The aim of this project is to understand the heterogeneity of both the immune consequences and treatment responses in CS. We will explore this heterogeneity through identification of transcriptomic sub-phenotypes and their association with outcomes, including therapeutic responses.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * All of the following are required for inclusion following screening: * Willing to provide informed consent or appropriate consent from a nominated consultee or personal consultee * Presentation within 24 hours of onset of ACS symptoms. * CS can only be secondary to ACS …
Contacts

Alastair Proudfoot

02037658707

alastair.proudfoot1@nhs.net

CONTACT

Mervyn Andiapen

02037658707

mervyn.andiapen@nhs.net

CONTACT