Actively Recruiting
Airway Coach Project: Prediction of Videolaryngoscopy Strategy With Clinical and Ultrasound Parameters (Multicentric)
Led by Clinica Universidad de Navarra, Universidad de Navarra ยท Updated on 2026-04-15
210
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
C
Clinica Universidad de Navarra, Universidad de Navarra
Lead Sponsor
C
County Clinical Emergency Hospital Cluj-Napoca
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating how clinical and ultrasound measurements can help predict the best videolaryngoscopy strategy for adults undergoing intubation during anesthesia or critical care. This observational, multicenter study aims to analyze data using artificial intelligence, including statistical and machine-learning methods, to understand how these measurements relate to videolaryngoscopy outcomes. The goal is to develop decision-support tools to assist clinicians, though these tools will not replace medical judgment. The study collects clinical parameters, demographic information, and point-of-care airway ultrasound measurements from adult patients undergoing general anesthesia with videolaryngoscopy intubation. Various ultrasound measurements, such as distances from skin to anatomical landmarks and tongue thickness, are taken immediately before anesthesia induction. Additional clinical airway assessments like the Modified Mallampati Score and neck circumference are also recorded. Participants will undergo ultrasound and clinical airway evaluations before anesthesia induction. Researchers will measure specific distances and thicknesses with ultrasound probes and record physical airway assessment scores. The study will analyze these results to predict difficult videolaryngoscopy. Data collection supports the creation of predictive models, and participant involvement lasts through the scheduled surgery requiring intubation, with no treatment or intervention changes required.
CONDITIONS
Brief Title
Airway Coach Project: Prediction of Videolaryngoscopy Strategy With Clinical and Ultrasound Parameters (Multicentric)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 and 90 years
- Both male and female patients
- ASA physical status I to III
- Scheduled surgery requiring orotracheal intubation
- Signed informed consent authorizing study participation
You will not qualify if you...
- Obesity class II, defined as a BMI greater than 35
- Pregnant individuals
- Presence of cervical tumors, goiter, or prior cervical radiotherapy
- Anatomical abnormalities such as facial or cervical fractures
- Maxillofacial abnormalities
- Individuals unable to provide consent
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 - Single day
Participants undergo clinical airway assessments and point-of-care airway ultrasound measurements immediately prior to induction of anesthesia to collect data for videolaryngoscopy planning.
1 visit (in-person) immediately prior to induction of anesthesia
Duration - Day of surgery
Participants who undergo routine anesthesia and videolaryngoscopy intubation are observed as part of standard care to collect outcome data.
Observation during surgery
Trial Site Locations
Total: 1 location
1
Clinica Universidad de Navarra
Madrid, Madrid, Spain, 28027
Actively Recruiting
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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