Persistent Platelet Reactivity in Acute Coronary Syndrome

Status Recruiting

Clinical Trial Summary

Study of persistent platelet reactivity during acute coronary syndrome. Patients are included at admission to the hospital. Platelet aggregation is evaluated by platelet function testing after blood sampling during hospitalization. No changes in treatment is planned.

Clinical Trial Description

Blood samples are performed on day 2 and 4 and collected with usual blood samples and analyzed by the laboratory. Maximal aggregation intensity and velocity are measured by light transmission aggregometry induced by arachidonic acid (AA) or adenosine diphosphate (ADP). Platelet function analyzer will be also used. No changes in treatment in response to the results is planned. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02038309
Study type	Observational [Patient Registry]
Source	Hopital Lariboisière
Contact
Status	Recruiting
Phase	N/A
Start date	January 2013
Completion date	December 2015

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