A 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/Actively Recruiting
Led by Universitätsklinikum Hamburg-Eppendorf · Updated on 2025-05-06
313
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying airway management challenges during anesthesia, focusing on awake tracheal intubation using flexible bronchoscopes ATIFB. 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 ATIFB and another to predict difficulty before the procedure. It also explores using machine learning to assess ATIFB. The study is observational and involves patients with anticipated difficult airways scheduled for ATIFB. 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 ATIFB 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 ATIFB or who are pregnant or breastfeeding.
CONDITIONS
Classification and Prediction of Difficult Awake Tracheal Intubation With Flexible Bronchoscopes
M
Martin Petzoldt, MD, FEAMS
V
Vera Köhl, MD
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Universitätsklinikum Hamburg-Eppendorf
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 hour
Participants undergo awake tracheal intubation using flexible bronchoscopes to assess airway management difficulty.
1 visit (in-person)
Duration - Up to 1 hour
Participants are observed for any airway-related complications and outcomes following the procedure.
1 follow-up visit (in-person)
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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Lead Sponsor