Coronavirus Infection
Conditions
Brief summary
Multicenter observational/registry study of the clinical features and outcomes of critically ill patients with COVID-19.
Detailed description
The goals of this project are to determine the independent risk factors for hospital mortality and acute organ injury, and to identify treatment strategies associated with improved survival. Additionally, we will assess outcomes according to differences in geographic and institutional parameters.
Interventions
OTHERNo intervention
Observational
Sponsors
Icahn School of Medicine at Mount Sinai
Montefiore Medical Center
Baylor College of Medicine
Baylor Health Care System
Beth Israel Deaconess Medical Center
University of Colorado, Denver
Cook County Hospital
The Cooper Health System
Duke University
Georgetown University
Hackensack mountainside hospital
Hackensack Meridian Health
Indiana University Health Methodist Hospital
Johns Hopkins University
Loma Linda University
Mayo Clinic
Medical College of Wisconsin
Northwestern University
Weill Medical College of Cornell University
NYU Langone Health
Ochsner Health System
Oregon Health and Science University
Renown Health
Rush University Medical Center
New Jersey Medical School
Rutgers Robert Wood Johnson Medical School
Stanford University
Temple University
Tufts Medical Center
Tulane University
University of California, Davis
University of California, Los Angeles
University of California, San Diego
University of California, San Francisco
University of North Carolina, Chapel Hill
University Hospitals Cleveland Medical Center
University Medical Center of Southern Nevada
University of Alabama at Birmingham
University of Chicago
University of Florida
University of Illinois at Chicago
University of Kentucky
University of Miami
University of Michigan
University of Oklahoma
University of Pennsylvania
University of Pittsburgh Medical Center
University of Tennessee
University of Washington
University of Texas, Southwestern Medical Center at Dallas
Yale University
Brigham and Women's Hospital
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
(each of the following): 1. Adults (aged ≥18 years) 2. Laboratory-confirmed diagnosis of COVID-19 3. Hospitalized in the ICU for illness related to COVID-19
Exclusion criteria
-None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 28-Day Mortality | 28-days from the day of ICU admission |
Secondary
| Measure | Time frame |
|---|---|
| 60-Day Mortality | 60-days from the day of ICU admission |
| 90-Day Mortality | 90-days from the day of ICU admission |
Countries
United States
Outcome results
None listed