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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05092737
Other study ID # Prone_COVID
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 1, 2021
Est. completion date April 30, 2022

Study information

Verified date October 2021
Source University of Lausanne Hospitals
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective study in COVID-19 ARDS patients hospitalised in the ICU. Investigators aim to explore the effects of prone positioning on oxygenation, dead space ventilation and mortality.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date April 30, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - COVID-19 associated moderate to severe ARDS - Invasive mechanical ventilation - Prone positioning - admitted to ICU Exclusion Criteria: - already sustained prone positioning in referring hospital - pronation during ECMO only - denied consent for data analysis

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Prone positioning
Prone position during invasive mechanical ventilation

Locations

Country Name City State
Switzerland Lausanne University Hospitals Lausanne Vaud

Sponsors (1)

Lead Sponsor Collaborator
University of Lausanne Hospitals

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary PaO2/FiO2 Arterial partial pressure of oxygen / Fraction of inspired oxygen Within 2 hours before pronation and 2 hours before supination
Secondary Alveolo-arterial oxygen gradient change Within 2 hours before pronation and 2 hours before supination
Secondary Ventilatory Ratio Within 2 hours before pronation and 2 hours before supination
Secondary Mortality or Extracorporeal membrane oxygenation (ECMO) support Once between ICU admission and extubation
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