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Pilot Study on the Use of Video Laryngoscopy in Pre-hospital Settings (VIDEOPREHOSP)

3. juni 2026 opdateret af: Centre Hospitalier de Valenciennes

Pilot Study on the Use of Video Laryngoscopy in Pre-hospital Settings: Evaluation of the Success Rate of Intubation on the First Attempt, Highlighting Criteria Specific to the Patient, the Practitioner and the Environment That May Influence This Rate.

Management of the upper airways is an essential skill in pre-hospital medicine in order to protect the respiratory tract and optimise ventilation and oxygenation. Orotracheal intubation remains the gold standard method in this context. In France, approximately 8% of primary SMUR interventions require intubation, representing 40,000 to 50,000 procedures per year, 30 to 40% of which are performed on patients in cardiorespiratory arrest.

Despite an overall success rate of nearly 99%, 8 to 15% of intubations are considered difficult and the success rate on the first attempt is only 77.8%. Difficult intubations expose patients to significant complications, including desaturation (nearly 50% of cases), haemodynamic disorders and, more rarely, cardiopulmonary arrest (3% of cases). Pre-hospital conditions (environment, access to the patient, trauma, secretions, etc.) increase these risks. As a result, recent recommendations now consider any emergency intubation outside the operating theatre to be potentially difficult.

The introduction of video laryngoscopy represents a major technological advance. Its superiority has been demonstrated in hospital settings, particularly for difficult intubations, and it is now recommended as the first-line treatment in this context. However, unlike in the United States, where several studies suggest that it is safer and more effective than direct laryngoscopy, there are no specific recommendations or French studies concerning its use in pre-hospital medicine.

Given these factors and the lack of national data, it seems appropriate to conduct an exploratory French study to assess the place, effectiveness, benefits and constraints of video laryngoscopy in a pre-hospital setting. Investigator hypothesises that the success rate for the first attempt at intubation using video laryngoscopy will be 74%.

Studieoversigt

Status

Rekruttering

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

This is a single-arm exploratory interventional study conducted at the Valenciennes Hospital Centre.

Firstly, practical training in video laryngoscopy has already been provided by Dr GOZE to doctors participating in the SMUR (mobile emergency and resuscitation service) at the Valenciennes Hospital Centre. In Appendix 1, the training certificates of the doctors who submitted their CVs during the initial application process have been included in the protocol. Any investigator wishing to participate in the study and include patients will be required to undergo training and submit an application to the CPP. A presentation of the study will also be given to practitioners.

Before the study is conducted, an explanatory sheet will be given to each practitioner, along with a questionnaire concerning their practice and experience of video laryngoscopy intubation.

From the start of the study, once authorisation has been granted by the CPP, all out-of-hospital intubations will be performed as a first-line treatment using a video laryngoscope, as required by the research protocol. If intubation fails on the first attempt, the practitioner will be free to choose whether to continue with the intubation technique of their choice.

A results sheet will be completed by the operator after each procedure. The results recorded will be: the outcome of the first intubation attempt (success or failure), and the criteria corresponding to the secondary criteria described above.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

143

Fase

  • Ikke anvendelig

Kontakter og lokationer

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Studiekontakt

Studiesteder

  • Frankrig
      • Valenciennes, Frankrig, 59300
        • Rekruttering
        • Centre Hospitalier de Valenciennes
        • Kontakt:
          • Alexandre ANDRIES, MD

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Patient Inclusion Criteria:

  • Age > 18 years
  • Patients treated pre-hospital by a team from the Emergency Medical and Resuscitation Service (SMUR) at Valenciennes Hospital 2025-A02374-45_SUMMARY_v1.1 dated 04/12/2025 _VIDEOPREHOSP Page 3 of 4
  • Patients whose condition requires pre-hospital orotracheal intubation
  • Patient or relative who has given consent for inclusion
  • Patient affiliated with a social security scheme

Pratician Inclusion Criteria :

  • Practitioner at Valenciennes Hospital
  • Practitioner who is part of the EMS team

Exclusion Criteria:

  • Progressive pregnancy
  • Theoretical indication for orotracheal intubation but patient refuses invasive care, considered in this situation to be futile medical care
  • Insurmountable anatomical obstacle, in which case an emergency cricothyroidotomy or tracheotomy should be considered as the first line of treatment
  • Patients under guardianship or curatorship
  • Patients deprived of their liberty by court order

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Experimental arm
All patients in a pre-hospital emergency situation for whom videolaryngoscopy was performed on the first attempt.
Enhed: Videolaryngoscopy in first attempt in prehospital with AirTraq

This is a single-centre study conducted at Valenciennes Hospital. Eligible patients will be those requiring intubation in a life-threatening emergency as part of standard care.

During each SMUR intervention, patients will be assessed to determine their eligibility for the study, according to the inclusion and exclusion criteria previously defined in the protocol. This verification will be carried out by the practitioner in charge of pre-hospital care, before the intubation procedure is performed. The clinical data required for this assessment will be collected prospectively.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The main objective of this exploratory study is to estimate the success rate of the first attempt at pre-hospital video laryngoscopy intubation.
Tidsramme: immediately after orotracheal intubation
The primary endpoint is the success rate of intubation on the first attempt. The endpoint analysed will be a binary measure (success: 1 / failure: 0) collected during the procedure.
immediately after orotracheal intubation

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Secondary objective N°1 : To study the correlation between patient-related constraints in the use of video laryngoscopy and the success/failure of the first intubation attempt.
Tidsramme: immediately after orotracheal intubation

The aim is therefore to study the main variable (success or failure of intubation on the first attempt) in relation to different variables that have different units of measurement.

Constraints encountered during intubation related to the patient:

  • Mouth opening: < 2 cm, between 2 and 3.5 cm, > 3.5 cm
  • Thyro-mental distance: < 5 cm, between 5 and 6.5 cm, > 6.5 cm
  • Cormack score: I/II, III/IV
  • Obesity (BMI > 30): Yes/No
  • Presence of secretions in the upper airways: Yes/No
  • Presence of cervical-facial trauma: Yes/No
immediately after orotracheal intubation
Secondary outcome N°2 : To investigate the correlation between the constraints of using video laryngoscopy in an out-of-hospital setting and the success/failure of the first intubation attempt
Tidsramme: immediately after orotracheal intubation

The aim is therefore to study the main variable (success or failure of intubation on the first attempt) in relation to different variables that have different units of measurement.

Constraints encountered during intubation, related to the practitioner:

  • Years of experience as an emergency physician
  • Number of successful intubations using video laryngoscopy: < 15, between 15 and 50, > 50
immediately after orotracheal intubation
Secondary objective N°3 : To investigate the correlation between the constraints of using video laryngoscopy in an out-of-hospital setting and the success/failure of the first intubation attempt
Tidsramme: Immediately after video laryngoscopy

The aim is therefore to study the main variable (success or failure of intubation on the first attempt) in relation to different variables that have different units of measurement.

Constraints encountered during intubation in an out-of-hospital setting:

  • Patient position: On the ground or on a stretcher
  • Practitioner position: Lying down, kneeling, or standing
  • Bright light interfering with visibility on the video laryngoscope: Yes or No
Immediately after video laryngoscopy

Samarbejdspartnere og efterforskere

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Sponsor

Centre Hospitalier de Valenciennes

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

2. januar 2026

Primær færdiggørelse (Anslået)

2. december 2026

Studieafslutning (Anslået)

2. december 2026

Datoer for studieregistrering

Først indsendt

6. januar 2026

Først indsendt, der opfyldte QC-kriterier

3. juni 2026

Først opslået (Faktiske)

5. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

5. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. juni 2026

Sidst verificeret

1. januar 2026

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 2025-02-03

Plan for individuelle deltagerdata (IPD)

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