Actively Recruiting

All Genders
ID06374030

A Retrospective Study on the Practice and Safety of Airway Management in Dutch Emergency Departments

Led by Frisius Medisch Centrum · Updated on 2024-07-03

1000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

F

Frisius Medisch Centrum

Lead Sponsor

V

VieCuri Medical Centre

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research explores how endotracheal intubation is practiced in emergency departments (EDs) across the Netherlands. It aims to describe patient details, reasons for intubation, who performs the procedure, the equipment and medications used, and any complications that occur. The study addresses a gap in knowledge about intubation safety and outcomes in Dutch EDs, comparing local practices with international data to improve patient safety. The study reviews all endotracheal intubations performed in participating Dutch EDs from January 1, 2019, to December 31, 2023. It collects detailed information from electronic patient records about each intubation event. This retrospective observational study does not involve interventions or treatments but analyzes existing data on the procedures carried out during this period. Participants are patients who underwent intubation in the listed timeframe. Researchers will examine complications occurring during and within one hour after the intubation procedure. The study relies on patient chart information to gather data on demographics, indications, provider characteristics, methods, and safety outcomes. There is no direct patient involvement or follow-up, and the study concludes after reviewing records up to the end of 2023.

CONDITIONS

Brief Title

Retrospective Study of Airway Management in Dutch ED's

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who underwent endotracheal intubation between 01-01-2019 and 31-12-2023 in the participating emergency departments
Not Eligible

You will not qualify if you...

  • Patients without available information about the intubation in their electronic patient chart will be excluded from the study

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.

No visits required; retrospective data review only

Diagnostic Evaluation

Duration - Retrospective from January 2019 to December 2023

Participants' medical records of endotracheal intubation in emergency departments are reviewed to assess the methods and safety of the procedure.

No visits required; data collection from past records

Long-term Monitoring

Duration - Within 1 hour post intubation

Participants' data on complications occurring during and within one hour after endotracheal intubation are analyzed.

No visits required; retrospective data analysis

Trial Site Locations

Total: 1 location

1

Leeuwarden Medical Centre

Leeuwarden, Netherlands, 8934AD

Actively Recruiting

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Research Team

P

Peter Veldhuis, 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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