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Enrolling by invitation Observational

Pre-hospital Ventilation Clinical Study

NCT05604430 · tracked via the Priya Life Science USA tracker
Phase
Observational
Started
2022-06-30
Last updated
2026-09-01

Condition(s) studied

Altered Mental StatusSepsisHeart FailureHemorrhageRespiratory Distress Syndrome, AdultCardiac Arrest

Investigational drug(s) / intervention(s)

731 Series Ventilator

731 Series Ventilator: FDA cleared ventilator indicated for use in the management of acute or chronic respiratory failure or during resuscitation.

Study summary

This study will collect and characterize ventilator use during patient care with a ZOLL 731 Series ventilator in a pre-hospital setting.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Candidates for this study must meet all of the following Inclusion criteria: 1. Ventilated using ZOLL 731 Series ventilator with Release 5 (or greater) software 2. Data recorded in ventilator data file Exclusion Criteria: * None

Primary outcome measure(s)

  • Ventilator modes used — Through study completion, an average 1 hour
    Characterizing how often ventilator modes are used during mechanical ventilation
  • Ventilator settings used — Through study completion, an average 1 hour
    Characterizing how often ventilator settings are changed during mechanical ventilation
  • Ventilator Alarm type — Through study completion, an average 1 hour
    Characterize type of alarms triggered during mechanical ventilation
  • Ventilator Alarm Frequency — Through study completion, an average 1 hour
    Characterize frequency of alarms triggered during mechanical ventilation

Trial sites (5)

FacilityCityRegionStatus
Aetna Ambulance Service, Inc Hartford Connecticut
East Baton Rouge EMS Baton Rouge Louisiana
Uxbridge Fire Uxbridge Massachusetts
MedStar Fort Worth Texas
Gig Harbor Fire Department Rosedale Washington

More Zoll Medical Corporation trials in the USA

AED 3 Post-Approval Study Active, not recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05604430 on ClinicalTrials.gov ↗ ← All trials in the USA