The Effect of the Covid-19 Pandemic Among Operated Patients

ConditionsCovid19Surgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorKarolinska Institutet

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 volunteers

Qualifiers

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 intervention

    The investigators will compare patients with/without confirmed COVID-19 infection

  • Socioeconomic status

    Other intervention

    Patients from different socioeconomic groups will be compared

Treatment groups

300,000 Participants
are divided into 3 treatment groups
Group 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 surgery

Secondary outcomes

1

Length of stay

Length of hospital stay

Time frame
Through study completion, an average of 1 month
2

Complications

Includes readmission, reoperation, infection, sepsis, respiratory failure, and number of days in the intensive care unit

Time frame
3 months post surgery

Other outcomes

Sponsors and contacts

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