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Clinical Trials/NCT05289141
NCT05289141
Completed
Not Applicable

Interest in the Use of Nasal High-Flow Oxygen Therapy (OptiFlow™) in Secondary Transport of COVID-19 Positive Patients

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer1 site in 1 country229 target enrollmentMarch 24, 2022
ConditionsCOVID-19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment
229
Locations
1
Primary Endpoint
Intubation rate
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Since the beginning of COVID-19 pandemic situation, several modes of ventilation have been tried to correct the hypoxaemia induced by SARS-CoV-2 virus. A few recent studies have concluded that high-flow nasal oxygen therapy (OptiFlow™) is beneficial in COVID-19. All mainly conclude that the use of OptiFlow™ avoid intubations and decrease hospitalization duration in critical care services.

At the emergency medical service 83 (SAMU 83), it has been decided to extend this ventilation mode during patient secondary transfers (transfer from an intensive care unit/other hospital unit/emergency department to another hospital's intensive care unit).

The emergency medical service 83 has equipped its intensive-care ambulances with OptiFlow™ in order not to interrupt this ventilation mode during transport.

The hypothesis is that patients with a severe respiratory form of COVID-19 transported from one health facility to another by the emergency medical service 83 on high-flow nasal oxygen therapy has a reduced risk of intubation compared to the other modes of non-invasive ventilation (NIV) and High Concentration oxygen Masks (HCM).

Detailed Description

Retrospective observational study in France including COVID-19 infected patients taken care of by the emergency medical service 83 (SAMU 83) for a secondary transport between1st March 2020 and 31th December 2021.

Registry
clinicaltrials.gov
Start Date
March 24, 2022
End Date
April 25, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • COVID-positive patient diagnosed either by positive Polymerase Chain Reaction (PCR) or radiological interpretation of chest CT
  • Patient in respiratory distress treated during transport by high flow nasal oxygen or HCM (with a minimum flow of 15 L/min) or other NIV modes
  • Patient taken care of by the emergency medical service 83 (SAMU 83) for secondary transport (transfer from an intensive care unit/other hospital unit/emergency department to another hospital's intensive care unit) between1st March 2020 and 31th December 2021

Exclusion Criteria

  • Pre-transport intubation
  • Patient opposition to participate in the study

Outcomes

Primary Outcomes

Intubation rate

Time Frame: 24 hours

Rate of intubation during the first 24 hours after arrival in the destination Intensive Care Unit (ICU)

Secondary Outcomes

  • Mortality rate(28 days)
  • ICU length of stay(At the moment of Intensive care unit discharge, up to 1 month)

Study Sites (1)

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