Pre-hospital Ventilation Clinical Study

ZOLL Medical

Status

Invitation-only

Conditions

Hemorrhage

Respiratory Distress Syndrome, Adult

Altered Mental Status

Heart Failure

Cardiac Arrest

Sepsis

Treatments

Device: 731 Series Ventilator

Study type

Observational

Funder types

Industry

Identifiers

NCT05604430

76701

Details and patient eligibility

About

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

Full description

This is a prospective, observational study.

ZOLL will develop a methodology to collect and transfer ventilator data from the device to ZOLL to allow for a characterization of ventilator use in the pre-hospital setting. This knowledge and experience will subsequently be used to inform development of a mechanism to allow for automatic data collection and transmission from ZOLL ventilators to a central data repository. These data will be used to provide feedback, reporting, and benchmarking to individual agencies and departments on their ventilator use as well as aggregate use data from all ventilators to allow for comparisons.

Enrollment in this study is expected to take approximately 24 months. No patient outcome data will be collected.Participants are enrolled once data have been downloaded from the ventilator via RescueNet® VentReview software. Participants will not be followed after the assessment of study objectives.

Enrollment

500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

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