Non Invasive Ventilation Comfort Study

Healthy Clinical Trial

Official title:

Non Invasive Ventilation Comfort Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02473068
• Other study ID #: CIA-170
• Status: Completed
• Phase: N/A
• Start date: June 19, 2015
• Est. completion date: June 4, 2019

Study information

• Verified date: June 2019
• Source: Fisher and Paykel Healthcare
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Patients who are suffering from a variety of respiratory conditions benefit from continuous positive airway pressure (CPAP) which is a form of Non-Invasive Ventilation (NIV). Some patients find the temperature of the breathing gas difficult to tolerate. The aim of this study is to compare comfort of healthy volunteer participants while being given CPAP at different temperatures.

Description:

Patients who are suffering from a variety of respiratory conditions benefit from continuous positive airway pressure (CPAP) which is a form of Non-Invasive Ventilation (NIV). Some patients find the temperature of the breathing gas difficult to tolerate. The aim of this study is to compare comfort of healthy volunteer participants while being given CPAP at different temperatures. Healthy volunteers will be given two different levels humidity and temperature and asked about preference.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: June 4, 2019
• Est. primary completion date: July 1, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 19 Years to 70 Years

Eligibility

Inclusion Criteria:

• Any employee of FPH willing to take part in the study following review of the Participant Information Sheet and who has provided affirmative answers to the questions / statements included on the Consent Form

Exclusion Criteria:

• Any employee of FPH not willing to take part in the study following review of the Participant Information Sheet.

• Any employee of FPH who has not provided affirmative answers to the questions / statements included on the Consent Form

Related Conditions & MeSH terms

• Healthy

Intervention

Device:
• CPAP

Locations

Country	Name	City	State
New Zealand	Fisher and Paykel Healthcare	Auckland

Sponsors (1)

Lead Sponsor	Collaborator
Fisher and Paykel Healthcare

Country where clinical trial is conducted

New Zealand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Participant Comfort Questionnaire	Participant answers questions to indicate comfort	30 Minutes