Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06528704

Impact of Real-Time Ventilation Feedback on Breathing Rate and Volume During Cardiac Arrest Using a Ventilation Feedback Device

Led by University Hospital, Ghent · Updated on 2025-01-15

100

Participants Needed

2

Research Sites

136 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research evaluates how real-time ventilation feedback affects ventilation rate and tidal volume during cardiac arrest. The study focuses on patients who are intubated and receiving manual resuscitation ventilation during out-of-hospital cardiopulmonary resuscitation. The purpose is to compare ventilation performance with and without feedback from a connected flow sensor. Patients are first ventilated without any feedback, although a flow sensor records ventilation data. Then, in a second cycle, the ventilation device displays real-time ventilation frequency and volume on a screen to inform the user. This device is being studied to see if showing this feedback changes how ventilation is delivered during cardiac arrest. Participants' ventilation frequency and volume are automatically recorded throughout the study. The main outcomes measured are delivered ventilation frequency and volume over 2-minute intervals. The study involves monitoring these parameters during the two ventilation cycles to assess the impact of feedback on ventilation during cardiac arrest.

CONDITIONS

Official Title

The Impact of Real Time Ventilation Feedback on Ventilation Rate and Tidal Volume During Cardiac Arrest.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years and older
Not Eligible

You will not qualify if you...

  • Traumatic cardiac arrest
  • Inability to intubate patient

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

AZ Zeno

Knokke, West-Vlaanderen, Belgium, 8301

Not Yet Recruiting

2

Ghent University Hospital

Ghent, Belgium

Actively Recruiting

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Research Team

M

Maxim Vanwulpen, MD

S

Said Hachimi-Idrissi, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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