Purpose

Researchers are creating a real time COVID-19 registry of current ICU/hospital care patterns to allow evaluations of safety and observational effectiveness of COVID-19 practices and to determine the variations in practice across hospitals.

Condition

Eligibility

Eligible Ages
All ages
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • COVID-19 PCR positive (within 7 days) - COVID-19 PCR pending - COVID-19 high clinical suspicion

Exclusion Criteria

  • Patient without Prior Research Authorization (applicable to Mayo Clinic sites) - Non COVID-19 related admissions - Repeated Admission to ICUs/Hospital

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Other

Arm Groups

ArmDescriptionAssigned Intervention
COVID19 test positive/pending or high clinical suspicion COVID19 test positive/pending/high clinical suspicion- patient admitted to hospital
  • Other: observational
    No Intervention
    Other names:
    • No Intervention

Recruiting Locations

More Details

NCT ID
NCT04323787
Status
Completed
Sponsor
Mayo Clinic

Detailed Description

Investigators aim is to create a real time COVID-19 registry of current ICU/hospital care patterns to allow evaluations of safety and observational effectiveness of COVID-19 practices and to determine the variations in practice across hospitals. Such a set of standards would increase the quality of single and multi-center studies, national registries as well as aggregation syntheses such as meta-analyses. It will also be of utmost importance in tiring times of public health emergencies and will help understand practice variability and outcomes during COVID-19 pandemic.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.