Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- All patients who undergo airway management in the ED involving endotracheal intubation
You will not qualify if you...
- Patients who undergo airway management outside the Emergency Department (e.g., operating room) will be excluded
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
Actively Recruiting
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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