Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Ignacio Saez de la Fuente
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.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patient above 18 year-old.
Diagnosis of severe ARDS due to COVID-19 under invasive mechanical ventilation,
Meet criteria for PP: PaO2/FiO2 \< 150 millimeters of mercury column (mmHg), PEEP ≥ 5 Centimeters of Water (cmH2O), FiO2 ≥ 60.
You may not be if
No consent for the study.
PP contraindicated (( elevated intracranial pressure, massive hemoptysis, recent tracheal surgery or sternotomy, unstable hemodynamic status, recent pacemaker implantation, severe facial laceration, open abdominal wound, spine, femur or pelvis fracture or pregnancy).
Clareo Health | Duration of Prone Position in the Severe Acute Respiratory Syndrome Coronavirus 2 (COVID-19).
