To evaluate the initial safety and effectiveness of the Ventor Airway System in providing short-term ventilation support in non-breathing subjects during cardiopulmonary resuscitation (CPR) and respiratory arrests.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Resuscitation with the Ventor device
Stony Brook University Hospital
Stony Brook, New York, United States
RECRUITINGAbility to provide oxygenation during CPR
As measured through the monitoring of intra-arrest PaO2
Time frame: From device insertion through 1 hour.
Ability to provide ventilation during CPR
As measured through the monitoring of intra-arrest PaCO2
Time frame: From device insertion through 1 hour
Ability to provide oxygenation during CPR
As measured through the monitoring of intra-arrest cerebral oximetry
Time frame: From device insertion through 1 hour
Number of participants with device-related adverse events
Number and rate of adverse events
Time frame: From device insertion through 3 months
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