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Clinical Trial Summary

There is no predictive tool for patients admitted to the emergency department with a suspicion of Covid-19 that will worsen secondarily and require a heavy lifting.

In a context of saturation of the healthcare system by the pandemic at Covid-19,it is essential to identify specific, accessible prognostic markers via minimally invasive sampling with low risk of infection for personnel caregiver, for optimal allocation of resuscitation resources.

This study proposes to evaluate the biological markers of routine care known to be associated with resuscitation admission in relation to hospitalization on conventional service for the prediction of worsening of patients admitted to the emergencies for Covid-19.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04341792
Study type Observational
Source University Hospital, Lille
Contact Delphine Garrigue, MD
Phone 03 20 44 67 97
Email Delphine.garrigue@chru-lille.fr
Status Recruiting
Phase
Start date April 11, 2020
Completion date April 2021

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