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PrediSuisse: Automatized Assessment of Difficult Airway

PrediSuisse: Automatized Assessment of Difficult Airway Using Three Videolaryngoscopes With the Help of Facial Recognition Techniques and Neural Network

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06453525
Acronym
PrediSuisse
Enrollment
1800
Registered
2024-06-11
Start date
2025-01-01
Completion date
2027-01-31
Last updated
2026-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Airway Complication of Anesthesia, Anesthesia, Intubation; Difficult or Failed

Keywords

Intubation, difficult airway, videolaryngoscopy

Brief summary

In the "PrediSuisse" research project, the investigators aim to create a reliable, reproducible, ultra-portable and radiation-free automatized software, able to identify automatically collected features, facial characteristics, and range of movements, to predict intubation difficulty. The software will generate a difficulty intubation score tailored to three commercially available videolaryngoscopes with different type of blades, corresponding to the predicted endotracheal intubation difficulty while providing the anaesthesiologist a reliable and non-subjective tool to assess individual patient's risks with regards to airway management.

Detailed description

The Swiss multi-institutional research project "PrediSuisse" aims to automatically predict and classify the difficulty of intubation and airway management using three commercially available videolaryngoscopes (VL) by acquiring face/profiles photos and sequences on a training set of 900 patients during the pre-anaesthesia consultation. For each patient, with the help of recently developed Machine Learning (ML), Artificial Intelligence (AI) and Convolutional Neural Network (CNN) techniques, a specially developed software will be trained to provide a predicted airway management difficulty index. This will be performed by correlating those photos/sequences and the real difficulty level of intubation, determined by three experts by reviewing the recordings of the intubations of the training set patients. The software will then be used in routine on a set of 900 other patients to validate the prediction performance.

Interventions

OTHERintubation

Tracheal intubation using one of the three existing videolaryngoscopes

Sponsors

Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients (≥ 18 years old) presenting at the pre-anesthesia consult for an elective general anesthesia necessitating a tracheal intubation * Signed informed consent.

Exclusion criteria

* Patients not speaking French (in Geneva and Lausanne) or Italian (in Lugano). * Patients previously operated on the airway with anatomical modifications (ENT Flaps, tracheotomies). * Patients unable to follow procedures or to give consent will also be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Software creation18 monthsThe primary outcome is to create a reliable, reproducible, ultra-portable and radiation-free automated software, capable of identifying automatically collected features such as facial characteristics, mouth opening, range of motion while moving the neck and thyromental distance to predict intubation difficulty. The identification of the difficult intubation score will be compared by the one goven independantly by three airway experts.

Secondary

MeasureTime frameDescription
Team Communication18 monthsThe secondary outcome is to evaluate the impact of streaming images of the intubations acquired by the videolaryngoscopy directly to the screens located in the operating room (OR) on communication between healthcare professionals in the OR with the help of a dedicated questionnaire.

Countries

Switzerland

Contacts

CONTACTPatrick Schoettker, PhD
patrick.schoettker@chuv.ch+41213142007
PRINCIPAL_INVESTIGATORPatrick Schoettker, PhD

Centre Hospitalier Universitaire Vaudois

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026