Comparison of three high flow oxygen therapy delivery devices

Not Applicable

Completed

• Conditions: Respiratory failure requiring critical care; Respiratory; Respiratory failure, not elsewhere classified

• Registration Number: ISRCTN15995925
• Lead Sponsor: Saint Eloi Hospital (Hôpital Saint Eloi) (France)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-09-20
• Last Update Posted: 7 November 2016

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

1. Consecutive patients = 18 years old hospitalized in a medical-surgical ICU
2. Planned removal of a tracheotomy tube previously placed in the ICU for weaning from mechanical ventilation

Exclusion Criteria

1. Pregnancy
2. Adult under tutelage
3. Contraindications for non-invasive ventilation, as defined by the last French consensus conference

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mean airway pressure measured in the trachea

Secondary Outcome Measures

Name	Time	Method
1. FiO2<br>2. Noise intensity<br>3. Respiratory and auditory discomfort