Investigate the Aerosol Particle Distribution During Aerosol Generating Procedures
- Conditions
- Transmission, Patient ProfessionalHigh-flow Nasal Cannula
- Registration Number
- NCT04353531
- Lead Sponsor
- Rush University Medical Center
- Brief Summary
Massive number of clinicians were infected during the outbreak of COVID-19, which raised the concerns of utilizing "aerosol generating procedures", particularly the use of high-flow nasal cannula, noninvasive ventilation, intubation, bronchoscopy examination and pulmonary function test. There appears to be a trend to avoid those treatments. Instead, aggressive intubation might cause shortage of medical devices and add extra workload. Therefore, we aimed to do a clinical observational study to evaluate the aerosol generation in these procedures and explore the potential measures to reduce the aerosol generation or dispersion.
- Detailed Description
The intent is to monitor exhaled aerosol produced by COVID-19 patients pre and post aerosol generating procedures. Monitoring will occur at a distance of 1 and 3 feet from the subject's airway. This observational study will be conducted in standard patient hospital rooms (standard or negative pressure room).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 15
• Adult patients who are diagnosed as COVID-19 infection in ICU or Adult patients are indicated for pulmonary function tests
• No need for any respiratory therapy
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The virus load in the air sample pre procedure/treatment at 1 foot away from patient 1 hour before procedure/treatment The virus load in the air sample pre procedure/treatment at 1 foot away from patient's airway in the patient's room
The aerosol mass/count concentration and virus load in the air sample during procedure/treatment at 1 foot away from patient during procedure/treatment The aerosol mass/count concentration and virus load in the air sample during procedure/treatment at 1 foot away from patient's airway in the patient's room
The aerosol mass/count concentration post procedure/ treatment at 1 foot away from patient 5 minutes post procedure/treatment The aerosol mass/count concentration post procedure/ treatment at 1 foot away from HFNC in the patient's room
The aerosol mass/count concentration pre procedure/treatment at 3 feet away from patient 5 minutes before procedure/treatment The aerosol mass/count concentration pre procedure/treatment at 3 feet away from patient's airway in the patient's room
The aerosol mass/count concentration pre procedure/treatment at 1 foot away from patient 5 minutes before procedure/treatment The aerosol mass/count concentration pre procedure/treatment at 1 foot away from patient's airway in the patient's room
The virus load in the air sample during/after procedure/treatment at 1 foot away from patient 1 hour during/after procedure/treatment The virus load in the air sample during/after procedure/treatment at 1 foot away from patient's airway in the patient's room
The aerosol mass/count concentration during procedure/ treatment at 3 feet away from patient during procedure/treatment The aerosol mass/count concentration during procedure/ treatment at 3 feet away from HFNC in the patient's room
The aerosol mass/count concentration 5 mins post procedure/ treatment at 3 feet away from patient 5 minutes post procedure/treatment The aerosol mass/count concentration 5 mins procedure/ treatment at 3 feet away from HFNC in the patient's room
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Rush university medical center
🇺🇸Chicago, Illinois, United States