Feasibility of a single-prong nasal cannula to deliver Nasal High Flow therapy in healthy volunteers

Not Applicable

Completed

• Conditions: Respiratory distress; Respiratory failure; Chronic obstructive pulmonary disease; Respiratory - Chronic obstructive pulmonary disease; Respiratory - Other respiratory disorders / diseases

• Registration Number: ACTRN12618000458235
• Lead Sponsor: Fisher and Paykel Healthcare

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-03-29
• Study Completion: 2018-05-10
• Last Update Posted: 15 July 2019

Recruitment & Eligibility

• Status: Completed
• Sex: Male
• Target Recruitment: 5

Inclusion Criteria

1. Between 18 and 40 years of age
2. Male
3. No diagnosis of sleep or respiratory conditions
4. Successfully passed a medical check-up for pre-existing sleep or respiratory conditions
5. Low score on the ‘Stop-Bang Sleep Apnoea Questionnaire’

Exclusion Criteria

1)Under 18 years of age
2)Female
3)Existence of sleep or respiratory conditions such as sleep apnea and asthma or allergies

Study & Design

• Study Type: Interventional
• Study Design: Not specified