Prospective development and validation of a universal classification for paediatric videolaryngoscopic tracheal intubation: the PeDiAC score.
Thorsten Dohrmann, Nelly Gutsche, Rilana Kramer...
https://pubmed.ncbi.nlm.nih.gov/39108225Actively Recruiting
Age: 18Years +
All Genders
ID06953414
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
N/A
Total Duration
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AI-Summary
What this Trial Is About
Researchers are studying airway management challenges during anesthesia, focusing on awake tracheal intubation using flexible bronchoscopes (ATI:FB). This method helps manage difficult intubations while patients breathe spontaneously. The study aims to develop and validate two prediction models: one to classify difficulty after ATI:FB and another to predict difficulty before the procedure. It also explores using machine learning to assess ATI:FB. The study is observational and involves patients with anticipated difficult airways scheduled for ATI:FB. There are no interventional treatments; instead, researchers will observe and collect data during the procedure. The focus is on evaluating airway management techniques and their outcomes. Participants will undergo ATI:FB as part of their scheduled care, during which data on procedure difficulty, success rates, timing, oxygen levels, cardiovascular events, and patient discomfort will be recorded within one hour. Researchers will use these observations to develop prediction models and assess related airway complications. The study includes consented adult patients and excludes those not scheduled for ATI:FB or who are pregnant or breastfeeding.
CONDITIONS
Brief Title
Classification and Prediction of Difficult Awake Tracheal Intubation With Flexible Bronchoscopes
Who Can Participate
Age: 18Years +
All Genders
Eligibility Criteria
You may qualify if you...
- Patients with an anticipated difficult airway scheduled for awake tracheal intubation using flexible bronchoscopes
- Consent given by the patient
- Minimum 18 years of age
You will not qualify if you...
- Patients not scheduled for awake tracheal intubation using flexible bronchoscopes
- Pregnant or breastfeeding patients
- Consent not given by the patient
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Diagnostic Evaluation
Duration - Up to 1 hour
Participants undergo awake tracheal intubation using flexible bronchoscopes to assess airway management difficulty.
1 visit (in-person)
Long-term Monitoring
Duration - Up to 1 hour
Participants are observed for any airway-related complications and outcomes following the procedure.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
University Medical Center Hamburg-Eppendorf
Hamburg, Free and Hanseatic City of Hamburg, Germany, 20246
Actively Recruiting
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Research Team
M
Martin Petzoldt, MD, FEAMS
V
Vera Köhl, 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
0
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Published Research Related To This Trial
Transnasal Videoendoscopy for Preoperative Airway Risk Stratification: Development and Validation of a Multivariable Risk Prediction Model.
Alexander Barclay-Steuart, Hanna L Großhennig, Phillip Sasu...
https://pubmed.ncbi.nlm.nih.gov/37074950A model to predict difficult airway alerts after videolaryngoscopy in adults with anticipated difficult airways - the VIDIAC score.
E K Kohse, H K Siebert, P B Sasu...
https://pubmed.ncbi.nlm.nih.gov/36006056