Overview
This is a longitudinal, multi-center, observational study collecting diverse biological measurements and clinical and epidemiological data for the purpose of enabling a greater understanding of the onset of severe outcomes, primarily acute respiratory distress syndrome (ARDS) and/or mortality, in patients presenting to the hospital with suspicion or diagnosis of COVID-19. We seek to understand whether there are early signatures that predict progression to ARDS, mortality, and/or other comorbid conditions. The duration of the study participation is approximately 3 months.
Eligibility
Inclusion Criteria:
- Participant or legally authorized representative willing and able to provide informed consent
- Receiving care at a participating hospital
- Age 21 years old or older
- U.S. Resident
- Patient classified as a Person Under Investigation (PUI) for COVID-19 or is confirmed positive for COVID-19
- Willing and able to comply with all study procedures
Exclusion Criteria:
- Pregnancy