AirSpiral and tracheostomy connector usability with myAIRVO 2

Completed

• Conditions: Chronic obstructive pulmonary disease; Requirement for Tracheostomy; Bronchiectasis; Respiratory - Chronic obstructive pulmonary disease; Respiratory - Other respiratory disorders / diseases

• Registration Number: ACTRN12616000286448
• Lead Sponsor: Fisher & Paykel Healthcare

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-03-04
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

Arm 1: At least 6 months but less than 18 years of age, current user of myAIRVO 2, expected to require heated humidification for a tracheotomy for more than 2 months.

Arm 2: 18 years or older, current user of myAIRVO 2, expected to use myAIRVO 2 for 2 months or longer.

Exclusion Criteria

Any condition that at the investigator discretion is believed may present a safety risk or impact the feasibility of the study or validity of the study results.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
sability of new breathing tube and tracheostomy connector will be evaluated by the user (participant or caregiver) using a 10-point Likert Scale rating.[After 2 months of use]

Secondary Outcome Measures

Name	Time	Method
Comfort of new heated breathing tube and tracheostomy connector will be evaluated by the user (participant or caregiver) using a 10-point Likert Scale rating.[After 2 months of use]