Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years and older
You will not qualify if you...
- Traumatic cardiac arrest
- Inability to intubate patient
AI-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
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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