Actively Recruiting
Classification and Prediction of Difficult Awake Tracheal Intubation With Flexible Bronchoscopes
Led by Universitätsklinikum Hamburg-Eppendorf · Updated on 2025-05-06
313
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Airway management problems are key drivers for anesthesia-related adverse events. Awake tracheal intubation using flexible bronchoscopes with preserved spontaneous breathing (ATI:FB) is a recommended technique to manage difficult tracheal intubation in anesthesia, intensive care and emergency medicine. However, a prospective developed classification for this type of airway management is lacking. Due to the absence of a specifically tailored, validated classification for awake intubation with flexible bronchoscopes, many airway operators and institutions use classification tools that were originally developed for direct laryngoscopy, such as the percentage of glottic opening (POGO) score or Cormack-Lehane classification, although their diagnostic performance for the classification of ATI:FB is unknown. This prospective model development and validation study aims to develop two multivariable prediction models: a diagnostic prediction model to classify difficult ATI:FB after ATI:FB has been performed and a second prognostic prediction model to predict the risk for difficult ATI:FB before ATI:FB is performed. An additional aim is to develop a machine learning algorithm to evaluate ATI:FB.
CONDITIONS
Official Title
Classification and Prediction of Difficult Awake Tracheal Intubation With Flexible Bronchoscopes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with an anticipated difficult airway scheduled for awake tracheal intubation using flexible bronchoscopes (ATI:FB)
- Consent given by the patient
- Minimum age of 18 years
You will not qualify if you...
- Patients not scheduled for awake tracheal intubation using flexible bronchoscopes (ATI:FB)
- Pregnant or breastfeeding patients
- Consent not given by the patient
AI-Screening
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Trial Site Locations
Total: 1 location
1
University Medical Center Hamburg-Eppendorf
Hamburg, Free and Hanseatic City of Hamburg, Germany, 20246
Actively Recruiting
Research Team
M
Martin Petzoldt, MD, FEAMS
CONTACT
V
Vera Köhl, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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