A reusable personalised ventilation hood: A phase 1 safety study of a new device (McMonty) in patients with suspected or confirmed COVID-19.
- Conditions
- Infectious respiratory diseases (COVID-19)Respiratory - Other respiratory disorders / diseasesInfection - Other infectious diseases
- Registration Number
- ACTRN12620000500954
- Lead Sponsor
- Western Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 20
Adult patients >18 years, being cared for in the intensive care unit, emergency department and general ward area, who are presumed or confirmed to have COVID-19.
Patients will be excluded from being cared for using the McMonty hood for any of the following reasons:
•Less than 18 years of age
•Pregnancy
•Displaying active signs of delirium
•History of dementia
•Patients deemed by healthcare staff to be at risk of injuring themselves or others due to mental illness, behaviour of concern or otherwise
•Patients known to suffer from claustrophobia
Additionally (& importantly), care of the patient using the McMonty Hood can be ceased (either temporarily or permanently) at any time if a patient indicates that they no longer wish to be enclosed by the hood.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method