Airway Coach Project: Prediction of Videolaryngoscopy Strategy With Clinical and Ultrasound Parameters (Multicentric)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorClinica Universidad de Navarra, Universidad de Navarra

About this trial

This multicentre observational study will collect clinical parameters, demographic data, and point-of-care airway ultrasound measurements from adult patients undergoing videolaryngoscopy across participating centres. The collected data will be analysed using artificial intelligence-based analytical approaches, including statistical and machine-learning techniques, to examine their association with predefined videolaryngoscopy-related outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients (male or female) ASA I-III, aged between 18 and 90 years, undergoing scheduled surgery requiring orotracheal intubation. The signature of the informed consent is required authorizing its inclusion in the study.

Disqualifiers

Obesity class II defined as a BMI greater than 35.

Pregnant.

Cervical tumors, goiter or patients who have required radiotherapy at the cervical level

Abnormalities that condition anatomy alterations such as facial / cervical fractures.

Trial population

Patients (male or female) ASA I-III, aged between 18 and 90 years, undergoing scheduled surgery requiring orotracheal intubation. The signature of the informed consent is required authorizing its inclusion in the study.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Ultrasound mesurements

    Diagnostic test

    Compare various clinical test with ultrasound parameters to predict difficult videolaryngoscopy intubation.

Treatment groups

210 Participants
are divided into 1 treatment group
Group A: Patient undergoing general anesthesia with videolaryngoscopy intubation1 intervention

Trial outcomes

Primary outcomes

1

Distance from skin to Hyoid bone measured with lineal ultrasound probe

Distance from skin to Hyoid bone measured with lineal ultrasound probe

Time frame
Immediately prior to induction of anesthesia
2

Distance from skin to epiglottis measured with lineal ultrasound probe

Distance from skin to epiglottis measured with lineal ultrasound probe

Time frame
Immediately prior to induction of anesthesia
3

Tongue Thickness measured with convex probe

Tongue Thickness measured with convex probe

Time frame
Immediately prior to induction of anesthesia
4

Distance from Jaw to Hyoid bone distance measured with convex probe

Distance from Jaw to Hyoid bone distance measured with convex probe

Time frame
Immediately prior to induction of anesthesia

Secondary outcomes

1

Modified Mallampati Score Class I: Soft palate, uvula, fauces, pillars visible. Class II: Soft palate, major part of uvula, fauces visible. Class III: Soft palate, base of uvula visible. Class IV: Only hard palate visible.

Modified Mallampati Score

Time frame
Immediately prior to induction of anesthesia
2

Thyromental distance measured from the thyroid notch to the tip of the jaw with the head extended

Thyromental distance

Time frame
Immediately prior to induction of anesthesia
3

Sternomental distance the distance from the suprasternal notch to the mentum and is measured with the head fully extended on the neck and the mouth closed

Sternomental distance

Time frame
Immediately prior to induction of anesthesia
4

Interincisor distance DIstance in centimeters between fornt incisors

Interincisor distance

Time frame
Immediately prior to induction of anesthesia

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Clinica Universidad de Navarra, Universidad de Navarra

Lead sponsor

County Clinical Emergency Hospital Cluj-Napoca

Collaborator

Hospital Ancona

Collaborator

Hospital CUF Porto

Collaborator