Chitotriosidase activity
Diagnostic TestThe chitotriosidase activity will be measured in all the subjects
NCT Number: NCT04752085
The aim of the cohort prospective observational study is to define the major factors influencing the course of COVID-19 infections and its prognosis in hospitalised patients.
The investigators plan to include 300 patients hospitalised with COVID-19 infection.
The phone contacts with patients are due after 90 and 180 days after discharge.
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Notify Me18 year and older
All sexes
Observational
University Hospital #1, Moscow, Russia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The chitotriosidase activity will be measured in all the subjects
Time frame: Up to 1 month
The primary endpoint is the need in biological therapy or/and respiratory support including noninvasive ventilation during hospital stay
Time frame: Up to 1 month
The investigators plan to assess the overall length of hospitalisation due to COVID-19 infection as an outcome measure
Time frame: 90 days
To assess the all-cause death 90 days after discharge
Time frame: 180 days
To assess the all-cause death 180 days after discharge
I.M. Sechenov First Moscow State Medical University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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