Actively Recruiting

All Genders
ID06558630

A Prospective Observational Cohort Study of Airway Management in Emergency Departments in the Netherlands

Led by Frisius Medisch Centrum · Updated on 2024-08-23

1000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to describe how airway management is performed in Emergency Departments (EDs) across the Netherlands, focusing on the procedure of endotracheal intubation. This technique is important in emergency care for patients with conditions like trauma, stroke, respiratory failure, or airway obstruction. While this intervention can save lives, it also carries risks such as airway injury, aspiration, low oxygen levels, low blood pressure, and cardiac arrest, which appear more frequently in EDs than in operating rooms. The study will collect data from as many Dutch ED centers as possible over several years, focusing on patients who undergo endotracheal intubation. This includes the planning, preparation, and execution of this procedure. The research will not involve treatment changes but will observe and record details about the process, including reasons for intubation and any complications. Participants will be patients who receive airway management in the ED. Researchers will monitor and record any adverse events occurring within 10 minutes after starting intubation, along with success rates of the first intubation attempt and the reasons for intubation. Data must be reported within 24 hours of the procedure. The study aims to improve understanding of airway management practices and support future quality improvements and research in Dutch emergency care.

CONDITIONS

Brief Title

ED Airway Management in the Netherlands.

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All patients who undergo airway management in the ED involving endotracheal intubation
Not Eligible

You will not qualify if you...

  • Patients who undergo airway management outside the Emergency Department (e.g., operating room) will be excluded

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to several years

Participants who undergo airway management in the Emergency Department are observed as data is collected on the planning, preparation, and execution of endotracheal intubation.

Data collected during and within 24 hours after intubation

Trial Site Locations

Total: 1 location

1

Leeuwarden Medical Centre

Leeuwarden, Netherlands, 8934AD

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Research Team

P

P Veldhuis, MD

J

J de Haan, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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