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Clinical Trial Summary

Aneurysmal subarachnoid haemorrhage is a complex pathology, the pathophysiology of which is still imperfectly understood. Its morbidity and mortality remain significant. In addition to the damage sustained by the brain in the immediate aftermath of aneurysmal rupture, which is inaccessible to life-saving treatment, a significant proportion of lesions occur at a distance from the initial event. Delayed cerebral ischaemia is one of the most morbid complications. It combines an inflammatory pattern with vascular dysfunction and neuronal excitotoxicity, leading to avoidable secondary neuronal loss. Vascular dysfunction is mediated by a loss of homeostasis between endothelial cells and figurative blood cells, including platelets. However, the interrelationship between these elements and the precise chronology of the dysfunction remain imperfectly described to date. It therefore seems appropriate to propose temporal monitoring of platelet activation kinetics over time, combined with concomitant collection of markers of endothelial damage, in order to clarify the vascular chronobiology of this pathology.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06375889
Study type Observational
Source Hospices Civils de Lyon
Contact Nicolas Chardon, MD;Msc
Phone 683396245
Email nicolas.chardon@chu-lyon.fr
Status Recruiting
Phase
Start date June 14, 2024
Completion date July 14, 2025

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