A comparison of high flow nasal oxygen to high flow face mask oxygen in recently extubated patients.

Completed

• Conditions: Hypoxia; Respiratory - Other respiratory disorders / diseases

• Registration Number: ACTRN12605000719639
• Lead Sponsor: Fisher and Paykel Healthcare

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2005-11-08
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Patients meeting extubation criteria whose families provide consent and later give delayed consent.

Exclusion Criteria

Patients who do not consent; patients with DNR order.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Arterial blood gas[Samples will be taken at 30 minutes after each time treatment has been given.]

Secondary Outcome Measures

Name	Time	Method
Endpoints include heart rate, blood pressure, respiratory rate, ability to tolerate mode (nurse assessed).[Secondary endpoints will be measured at the same time points as ABG sampling is performed.];Patient reported comfort will be obtained once the patient is able to talk clearly.[When patients are able to talk clearly]