Informazioni generali
  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento completato (BASEC/ICTRP)
  • Luogo dello studio
    Berna
    (BASEC)
  • Responsabile dello studio Thomas Riva thomas.riva@insel.ch (BASEC)
  • Fonte dati BASEC: Importato da 03.03.2026 ICTRP: N/A
  • Ultimo aggiornamento 03.03.2026 10:50
HumRes65106 | SNCTP000005927 | BASEC2024-D0041

Software-assisted placement of the ventilation tube: an observational study on the accuracy of the software's indications regarding the position of the ventilation tube

  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento completato (BASEC/ICTRP)
  • Luogo dello studio
    Berna
    (BASEC)
  • Responsabile dello studio Thomas Riva thomas.riva@insel.ch (BASEC)
  • Fonte dati BASEC: Importato da 03.03.2026 ICTRP: N/A
  • Ultimo aggiornamento 03.03.2026 10:50

Descrizione riassuntiva dello studio

With this study, we aim to analyze the function of the new CE-certified medical device Larynguide TM (aiEndoscopic, Zurich, Switzerland). This device, with an installed AI software, is used for the placement of the ventilation tube and for assessing the correct position of the ventilation tube. A study on models with Larynguide TM showed that AI-assisted placement of the ventilation tube by less experienced personnel can be successfully performed in a similar time as by experienced anesthetists. The newly developed software Larynguide TM aims to increase safety during the placement of the ventilation tube. Patients requiring general anesthesia with a ventilation tube during surgery at the University Hospital of Bern will be asked for their consent. The study is designed as an observational study: for all consenting patients, Larynguide TM will be used for the placement of the ventilation tube, provided that no exclusion criteria are present. This medical device does not differ, apart from the installed software, from the video spatulas we routinely use for the placement of the ventilation tube. Thus, participation in the study does not pose any additional risks to the patients. The aim of our observational study is to evaluate whether Larynguide TM can better judge and recognize the incorrect placement of the ventilation tube in humans thanks to the software, compared to the anesthetists themselves using a conventional video spatula. The anesthetist will use Larynguide TM for the placement of the ventilation tube, while judging for themselves whether the position of the ventilation tube is correct or not. Simultaneously, the study team will note the assessment from Larynguide TM. The induction of anesthesia is not delayed by the conduct of the study.

(BASEC)

Intervento studiato

We investigate the process of placing a ventilation tube. Patients undergoing surgery with general anesthesia must be artificially ventilated. A possible method of securing the airway is the insertion of a ventilation tube. This is inserted in the sleeping patient using a laryngoscope/video laryngoscope. A laryngoscope is a spatula used to visualize the larynx and vocal cords to introduce the ventilation tube into the airways under direct vision. A video laryngoscope has the additional function of displaying on a small screen (at the top of the spatula handle) a transmission from a camera located at the tip of the spatula, allowing the laryngoscopy to be observed not only by the person performing it but also by a supervisor. During the placement of the ventilation tube, there is a risk, despite visualizing the larynx, of mistakenly placing the ventilation tube in the esophagus. If an incorrect placement goes unnoticed, it can lead to death, as the patient cannot be ventilated. aiEndoscopic has developed a video laryngoscope with an installed AI software (Larynguide TM), which assesses during the placement of the ventilation tube whether the tube has been correctly placed. The software displays its assessment in real-time on the monitor of the video laryngoscope as "confirmation" or "warning". Thus, the rate of unnoticed placements of the ventilation tube in the esophagus should be able to be reduced.

(BASEC)

Malattie studiate

We investigate the placement of the ventilation tube, which is necessary to artificially ventilate patients. The health condition in which such an intervention is necessary arises when there is an indication for general anesthesia or generally for artificial ventilation (e.g., comatose state). Our research project does not focus on any specific disease but on an intervention applied across various clinical pictures.

(BASEC)

Criteri di partecipazione
Patients ≥ 18 years old ASA Class I-III Elective surgery under general anesthesia with ventilation tube (BASEC)

Criteri di esclusione
• Patients < 18 years old • Contraindication for the placement of the ventilation tube with a video laryngoscope • Expected difficult mask ventilation (BASEC)

Luogo dello studio

Berna

(BASEC)

non disponibile

Sponsor

Thomas Riva

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Thomas Riva

+41 31 632 27 25

thomas.riva@insel.ch

Inselspital

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione d'etica Berna

(BASEC)

Data di approvazione del comitato etico

30.05.2024

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
Artificial intelligence‐assisted tracheal intubation in humans: a prospective observational study of diagnostic accuracy (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile