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Duration of Prone Position in the Severe Acute Respiratory Syndrome Coronavirus 2 (COVID-19). — OmeLEtte  

Ards Clinical Trial

Official title:
OptiMal pronE Position LEnghT in Patients With acuTE Respiratory Distress Syndrome Due to COVID-19.

Clinical Trial Summary

The OMELETTE study is a randomised, controlled, unicentric, open-label study to prove the noninferiority of reduced prone position (PP) sessions (more tan 16 hours) versus prolonged PP (48 hours).

Clinical Trial Description

This is a non-comercial, investigator-driven clinical study developed in a single critical care unit. The study is coordinated by the main investigator from Hospital Universitario 12 de Octubre in Madrid; The sponsorship is performed by Dr. Ignacio Sáez (Hospital Universitario 12 de Octubre). The study was planned according to the Good Clinical Practices. Omelette study has been approved by the Ethics Committee. All participating Patients must give informed consent before any study procedure occur. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05012267
Study type Interventional
Source Hospital Universitario 12 de Octubre
Contact
Status Completed
Phase N/A
Start date March 25, 2021
Completion date October 27, 2021
View Details
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