The VENTOR Clinical Study

Part of paid clinical trials in Stony Brook, New York.

Sponsor
CoLabs Medical
Study ID
NCT06759389
Status
Recruiting
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Conditions

  • Cardiac Arrest (CA)

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • Resuscitation (Ventor) — DEVICE
    Resuscitation with the Ventor device

Study Details

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.

Key Dates

Start date
Apr 4, 2025
Status verified
Apr 2025
Primary completion
Jun 30, 2026
Completion
Jun 30, 2026

Study Design

Enrollment
25 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Ventor
    Subjects being treated with Ventor device

Primary Outcome Measure

Ability to provide oxygenation during CPR [ Time Frame: From device insertion through 1 hour. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Stony Brook University HospitalStony BrookNew York11794
Jacqueline Skarre
[email protected]
631-444-9033
Jignesh Patel, M.D., M.Sc. (PRINCIPAL_INVESTIGATOR)

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By research site
Stony Brook University Hospital· Stony Brook, NY

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