A mobile and reusable personalised ventilation hood: A phase 1 safety study of a new device in patients with suspected or confirmed COVID-19.

Not Applicable

Withdrawn

• Conditions: COVID-19; Tuberculosis; Influenza; Measles; Respiratory - Other respiratory disorders / diseases; Infection - Other infectious diseases

• Registration Number: ACTRN12622000553774
• Lead Sponsor: Western Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-04-11
• Last Update Posted: 19 April 2022

Recruitment & Eligibility

• Status: Withdrawn
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Inclusion criteria for patients
•Adult patients of at least 18 years, presenting to the ED, who are suspected or a respiratory infection that warrants the use of droplet and/or aerosol precautions.

Inclusion criteria for staff
•Any nursing, medical or allied health staff involved in the provision of care to the patient in this study.

Exclusion Criteria

•<18 years
•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 Mini Isolation 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