Aerosol Biocontainment Device (ABCD) with Aerosol Clearance for Aerosol Generating Procedures
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- STATUS
- Recruiting
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- participants needed
- 170
Summary
The primary goal of this study is to assess use of an aerosol biocontainment device for planned airway procedures under general anesthesia. This will serve as a platform for using this device as a novel biocontainment and aerosol evacuation system as part of rapid sequence intubation protocols for COVID-19 patients.
Description
FAQ
Details
| Condition | anesthesia,COVID19 |
|---|---|
| Age | 99years or below |
| Clinical Study Identifier | TX6474 |
| Last Modified on | 19 February 2024 |
Eligibility
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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