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Clinical Trials/NCT04372576
NCT04372576
Unknown
Not Applicable

Epidemiology and Outcome of Ventilator-associated Pneumonia Among Critically Ill COVID-19 Patients

Semmelweis University1 site in 1 country30 target enrollmentApril 16, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ventilator Associated Pneumonia
Sponsor
Semmelweis University
Enrollment
30
Locations
1
Primary Endpoint
28-day all-cause mortality
Last Updated
5 years ago

Overview

Brief Summary

The aim of this study is to determine the risk factors for development of ventilator-associated pneumonia (VAP) and to identify the prognostic factors of VAP among Coronavirus Disease 2019 (CoViD-19) patients. We hypothesized that CoViD-19 serves as a high risk factor for the development of VAP and it affects clinical outcome measures negatively.

Detailed Description

Coronavirus Disease 2019 (CoViD-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) became a pandemic affecting thousands of individuals worldwide. A considerable proportion of CoViD-19 patients require admission to the intensive care unit (ICU), although limited data are available on their clinical characteristics and course. The results of retrospective studies indicate older age, presence of comorbidies and secondary infections as predictors of mortality among this population. Further evaluation regarding ICU clinical course and predictors of mortality is needed. The aim of this study is to determine the risk factors for development of VAP and to identify the prognostic factors of VAP among CoViD-19 patients.

Registry
clinicaltrials.gov
Start Date
April 16, 2020
End Date
August 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Zsolt Iványi

Associate Professor

Semmelweis University

Eligibility Criteria

Inclusion Criteria

  • Critically ill individuals diagnosed with PCR confirmed CoViD-19 disease
  • Started mechanical ventilation for \> 48 hours
  • Informed consent signed by the patient or authorised representative

Exclusion Criteria

  • Participation in an interventional trial aiming nosocomial infections
  • refused informed consent

Outcomes

Primary Outcomes

28-day all-cause mortality

Time Frame: at study completion, anticipated 5 months

Secondary Outcomes

  • ICU length-of-stay(average time frame expected 3-4 weeks)
  • Days of mechanical ventilation(average time frame expected 2-3 weeks)
  • Antibiotic utilization(average time frame expected 3-4 weeks (at discharge from ICU))
  • Ventilator-associated pneumonia rate(at study completion, anticipated 5 months)

Study Sites (1)

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