A study on the effectiveness of an oxygen delivery system.

Completed

• Conditions: Healthy subjects; Respiratory - Normal development and function of the respiratory system

• Registration Number: ACTRN12605000798662
• Lead Sponsor: Fisher and Paykel Healthcare

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2005-12-20
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

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

Inclusion Criteria

Fit Healthy Adult Volunteers.

Exclusion Criteria

1. Pregnancy. 2. Abnormal upper airway anatomy. 3. Recent (within 1 week) or current upper or lower respiratory tract infection. 4. Chronic respiratory illness. 5. Any medical condition precluding the ability to exercise eg. exercise induced asthma, ischaemic heart disease, hypertrophic obstructive cardiomyopathy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
FETO2 at different flow rates.[Sampled continuously via the naso-hypopharyngeal catheter.];FETCO2 at different flow rates.[Sampled continuously via the naso-hypopharyngeal catheter.]

Secondary Outcome Measures

Name	Time	Method
Secondary outcomes include heart rate, blood pressure and respiratory rate.[These will be measured continuously and correlated to changes in flow rates.]