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NCT Number: NCT06453525

PrediSuisse: Automatized Assessment of Difficult Airway

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.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Lausanne CHUV

Lausanne, 1011, Switzerland

Location status: Recruiting

Location contact

Patrick Schoettker, PhD

CONTACT

[email protected]

+41213142007

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

intubation

Other

Tracheal intubation using one of the three existing videolaryngoscopes

Primary outcomes

  1. Software creation

    Time frame: 18 months

    The 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 outcomes

  1. Team Communication

    Time frame: 18 months

    The 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Patrick Schoettker, PhD

CONTACT

[email protected]

+41213142007

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Vaudois

Other

Registry information

Official study title

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

Acronym: PrediSuisse

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jun 11, 2024
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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