About this trial
This project covers several research aims and uses different research methods, such as cohort analyses.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients that undergo surgical treatment in the Stockholm Region during the study period
Disqualifiers
None
Trial population
Patients that undergo surgical treatment in the Stockholm Region during the study period
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
COVID-19 infection status
Other interventionThe investigators will compare patients with/without confirmed COVID-19 infection
Socioeconomic status
Other interventionPatients from different socioeconomic groups will be compared
Treatment groups
300,000 Participants
are divided into 3 treatment groupsGroup A: COVID-191 intervention
Group B: Non-COVID-191 intervention
Group C: Socioeconomic status1 intervention
Trial outcomes
Primary outcomes
1
Death
Mortality
Time frame
30 days post surgerySecondary outcomes
1
Length of stay
Length of hospital stay
Time frame
Through study completion, an average of 1 month2
Complications
Includes readmission, reoperation, infection, sepsis, respiratory failure, and number of days in the intensive care unit
Time frame
3 months post surgerySponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov