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The VENTOR Clinical Study

NCT06759389 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2025-06-11

No results posted yet for this study

Summary

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

  • Cardiac Arrest (CA)

Interventions

DEVICE

Resuscitation (Ventor)

Resuscitation with the Ventor device

Sponsors & Collaborators

  • CoLabs Medical

    lead INDUSTRY

Principal Investigators

  • Jignesh Patel, M.D., M.Sc. · Stony Brook University Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-04
Primary Completion
2026-06-30
Completion
2026-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06759389 on ClinicalTrials.gov