Impact of Aerosol Box Use During Cardiopulmonary Arrest: A Multicenter Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorKidSIM Simulation Program

About this trial

Aerosol Generating Medical Procedures (AGMP) are procedures that have the potential to create tiny particles suspended in the air. These particles can contain germs such as viruses. The Coronavirus Disease 2019 (COVID-19) pandemic was caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Patients infected with SARS-CoV-2 experience unusually high rates of critical illness that needs advanced airway management and intensive care unit admission. Bag-valve-mask (BVM) ventilation, endotracheal Intubation (ETI) and chest compressions are sometimes required for critically ill COVID-19 patients, and may contribute to a high risk of infection amongst Health Care Workers (HCW). To lessen HCW risk during high-risk procedures, a device called an aerosol box has been developed to place over the head of the patient, shielding the provider's face from virus droplets suspended in the air.

The purpose of this research study is to better understand how particles disperse during AGMPs, more specifically during the provision of cardiopulmonary resuscitation (CPR). The project team hopes what is learned from the project can help inform infection control measures. This could help make changes to the clinical environment and make it safer for HCW's. The investigators intend to explore how an aerosol box performs in reducing contamination of HCW's who perform critical airway interventions during resuscitation events.

Eligibility criteria

Qualifiers

Attending physician, fellow or resident in adult or pediatric emergency medicine, pediatric intensive care, general pediatrics or pediatric/adult anesthesia

Adult or Pediatric Advanced Life Support certification.

Attending physician, resident, fellow, nurse, respiratory therapist, physician assistant or health care aide

Basic Life Support, Adult or Pediatric Advanced Life Support certification

Disqualifiers

Decline to provide informed consent

Unable to perform tasks required of the role due to physical limitations.

Trial design

Treatments tested in this trial

  • Aerosol box

Treatment groups

240 Participants
are divided into 2 treatment groups

Sponsors and collaborators

KidSIM Simulation Program

Lead sponsor

University of Calgary

Sponsor institution

Canadian Institutes of Health Research (CIHR)

Collaborator