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New study aims to boost First-Attempt intubation success in the field

NCT ID NCT07630467

Knowledge-focused Sponsor: Centre Hospitalier de Valenciennes Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This pilot study tests whether using a video laryngoscope (a camera-equipped breathing tube device) helps doctors successfully intubate patients on the first try during emergencies outside the hospital. About 143 adults needing emergency intubation will be included. The goal is to measure success rates and identify factors like patient condition, doctor experience, and environment that affect outcomes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Video laryngoscopy device (AirTraq)
What this could lead to
If successful, this study could provide evidence that video laryngoscopy improves first-attempt intubation success in pre-hospital emergencies, potentially leading to updated guidelines and better patient outcomes.
What could go wrong
This is a small, single-center pilot study with no control group, so results may not apply broadly. The expected success rate is only 74%, and real-world conditions could lower it further.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 143 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Emergencies

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Emergency Orotracheal intubation

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Centre Hospitalier de Valenciennes

    RECRUITING

    Valenciennes, 59300, France

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