Evaluating Patient Comfort and Environmental Conditions in the Carecube Negative Pressure Isolation Chamber.1

CompletedOBSERVATIONAL
Enrollment

11

Participants

Timeline

Start Date

May 24, 2022

Primary Completion Date

June 18, 2022

Study Completion Date

June 18, 2022

Conditions
Infectious Diseases
Interventions
DEVICE

Carecube Negative Pressure Isolation Chamber

Subjects will be tasked to stay within the Carecube Isolation Chamber for at least 4 hours and have 3 consecutive timepoints illustrating a plateau level for all participants parameters. Environmental data will be collected by physicians and nurses \[which may include physicians, physician assistants, Registered Nurses, Licensed Practical Nurses, medical technicians and emergency medical technicians (EMTs)\] . Additionally, atmospheric Oxygen, Carbon Dioxide, humidity, and room temperature will be monitored and recorded on an hourly basis. External to the room humidity and temperatures will also be recorded. The participant will be exposed to room temperature (° Fahrenheit) and humidity (RH%), ranging from 65°- 90° Fahrenheit and 30%-60% RH. Participants will also be asked to record on a questionnaire, in order to demonstrate that the Carecube Negative Pressure Isolation chamber is a safe and non-hostile environment for the patients that will be contained during normal operations.

Trial Locations (1)

68198-8437

UNMC, Omaha

All Listed Sponsors
collaborator

University of Nebraska

OTHER

lead

Carecubes, Inc.

INDUSTRY