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Clinical Trial Summary

The aim of this PROJECT is to develop two biomarkers to assess the thrombotic and hemorrhagic risk of patients with chronic renal failure (CKD) treated with antiplatelet drugs following the occurrence of an acute coronary syndrome (ACS). These biomarkers will help to adapt antiplatelet therapy on an individual basis (intensity, duration of antiplatelet treatment) and thus reduce the risk of thrombotic and hemorrhagic events in this particularly fragile population. The methods for measuring these two highly innovative biomarkers are currently being developed. The first biomarker corresponds to the measurement of an intraplatelet molecule, Rap1b in its active form (aRap1b). The second biomarker is the measurement of the pro-antithrombotic balance of circulating endothelial microvesicles (patEMV), a reflection of endothelial dysfunction. An automated method for biomarker measurement will be developed in partnership with the industrial partners Stago and BioCytex during the project.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05765630
Study type Interventional
Source Assistance Publique Hopitaux De Marseille
Contact Stephane BURTEY, Pr.
Phone +33(0)634603257
Email stephane.burtey@univ-amu.fr
Status Recruiting
Phase N/A
Start date March 8, 2023
Completion date March 2024

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