Pre-hospital Ventilation Clinical Study

Heart Failure Clinical Trial

Official title: Pre-hospital Ventilation Clinical Study

Status Enrolling by invitation

Clinical Trial Summary

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

Clinical Trial 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. ;

Related Conditions & MeSH terms

• Acute Lung Injury
• Altered Mental Status
• Cardiac Arrest
• Heart Failure
• Hemorrhage
• Respiratory Distress Syndrome
• Respiratory Distress Syndrome, Adult
• Respiratory Distress Syndrome, Newborn
• Sepsis

• NCT number: NCT05604430
• Study type: Observational
• Source: Zoll Medical Corporation
• Status: Enrolling by invitation
• Start date: June 30, 2022
• Completion date: June 30, 2024