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Clinical Trials/NCT04649658
NCT04649658
Completed
Not Applicable

Awake Prone Position in Critical and Severe COVID-19 Patients Undergoing Noninvasive Respiratory Support: a Retrospective Multicenter Cohort Study

University of Modena and Reggio Emilia1 site in 1 country93 target enrollmentMarch 1, 2020
ConditionsCovid19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
University of Modena and Reggio Emilia
Enrollment
93
Locations
1
Primary Endpoint
Endotracheal intubation
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Pronation seems feasible and effective in improving blood oxygenation in patients with COVID-19 pneumonia. Data are lacking on the effects of pronation on clinical outcome in this subset of patients.

Registry
clinicaltrials.gov
Start Date
March 1, 2020
End Date
November 30, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Modena and Reggio Emilia
Responsible Party
Principal Investigator
Principal Investigator

Roberto Tonelli

MD

University of Modena and Reggio Emilia

Eligibility Criteria

Inclusion Criteria

  • Inclusion Criteria
  • patients aged ≥18 and \< 80 years old
  • acute respiratory failure

Exclusion Criteria

  • endotracheal intubation performed within the first 24 hours from admission,
  • ceiling of escalation of intensive care
  • do not intubate order as expressed by patient willing or upon clinical judgement
  • missing core data at medical record analysis (clinical features at baseline, pronation information, type and time of ventilatory support required, mortality, need for tracheostomy, length of respiratory intensive care unit and hospital stay).

Outcomes

Primary Outcomes

Endotracheal intubation

Time Frame: 28 days

Secondary Outcomes

  • Mortality(28 days)
  • Length of Respiratory Intensive Care Unit stay(60 days)
  • Length of Hospital stay(60 days)
  • Tracheostomy(28 days)

Study Sites (1)

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