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Prospective Observational Cohort Study of Critically Ill Patients With Covid-19 in Sweden

Completed
Conditions
Covid-19
Critical Illness
Interventions
Other: Observational study
Registration Number
NCT04382417
Lead Sponsor
Region Västmanland
Brief Summary

The study will prospectively collect data from patients with Covid-19 admitted to the Västerås Intensive Care Unit, Västerås Hospital. Demographic, clinical, radiographic and laboratory characteristics will be recorded. Analysis of data to identify predictors of disease severity, mortality and treatment response.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
57
Inclusion Criteria
  • Patients admitted to the Intensive Care Unit with biological samples positive for SARS-CoV-2.
  • Patients admitted to the Intensive Care Unit with one or more negative tests but with clinical and radiological characteristics highly suggestive of SARS-CoV-2 and thus considered positive for the disease.
Exclusion Criteria
  • None.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Covid-19Observational studyPatients with verified or highly suggestive Covid-19 diagnosis and Intensive Care treatment.
Primary Outcome Measures
NameTimeMethod
All-cause mortalityAt 90 days follow-up after admittance to Intensive Care
Secondary Outcome Measures
NameTimeMethod
Hospital length of stayUntil 90 days after admittance to Intensive Care
Number of days on mechanical ventilationUntil 90 days after admittance to Intensive Care
Number of patients receiving vasopressor supportUntil 90 days after admittance to Intensive Care
Number of patients receiving renal replacement therapyUntil 90 days after admittance to Intensive Care
ICU length of stayUntil 90 days after admittance to Intensive Care
Patient characteristicsAt admission to ICU

Trial Locations

Locations (1)

Intensive Care Unit, Västerås Hospital

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Västerås, Västmanland, Sweden

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