NCT04306107

Prone Position in Non-Invasive Ventilation and High-Flow Oxygen Therapy

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 100 (estimated)
• Sponsor: Hospital General Universitario Morales Meseguer · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The aim of this trial is to study the effect of prone position during NIV and HFNC on acute hypoxemic respiratory patients.

Detailed description

Inclusion Criteria: Adult patients with: • ARDS/pneumonia/acute hypoxemic respiratory failure with PaO2/FiO2 between 150 and 300 (on 5 cmH2O PEEP level) Exclusion Criteria * General NIV or HFNC contraindications * Immediate need for IOT * Prone position intolerance * Patients refusal to participate Interventions: * Prone position for 2-4 hours twice a day, for 3 days (first 3 days since admission to ICU) * Nurse surveilance: at least every 15 minutes Outcomes: * Need for IOT * Effects on the measurements specified above (particularly PaO2/FiO2)

Conditions

• Evaluation of Prone Position Effect During NIV and HFNC on Acute Hypoxemic Respiratory Failure

Interventions

Type	Name	Description
DEVICE	Prone position during non-invasive respiratory support	HFNC and NIV application with patient on prone position

Timeline

• Start date: 2021-09-01
• Primary completion: 2021-11-01
• Completion: 2022-05-01
• First posted: 2020-03-12
• Last updated: 2021-08-30