Actively Recruiting
The VENTOR Clinical Study
Led by CoLabs Medical · Updated on 2025-06-11
25
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The VENTOR Clinical Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18-75 years, inclusive
- Non-traumatic in-hospital cardiac arrest (IHCA)
- Height of at least 4 feet
You will not qualify if you...
- Intubated with an endotracheal tube
- Valid do-not-attempt-resuscitation (DNAR) or study opt-out bracelet
- Legal authorized representative or family objects to enrollment
- Obvious signs of irreversible death (rigor mortis, lividity, decapitation, transection, decomposition)
- Responsive with an intact gag reflex
- Injury from blunt trauma, penetrating trauma, burns, drowning, or electrocution
- Known upper airway foreign body or mass
- Lower airway obstruction
- Dental gap less than 2 cm
- Ingested caustic substances
- Incomplete medical history or history only completed by emergency physician
- Known esophageal disease or facial/perforating neck trauma, including esophageal varices, cancer, strictures
- Use of oxaliplatin, leucovorin, or fluorouracil medications
- History or evidence of vomiting blood or caput medusae
- Known vulnerable subjects such as prisoners, pregnant individuals, terminal illness, or dementia
- Medical, surgical, or other conditions limiting study participation per investigator's opinion
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Stony Brook University Hospital
Stony Brook, New York, United States, 11794
Actively Recruiting
Research Team
C
Clay Nolan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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