← Eichor
Study identifier: NCT06307392 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Bougie Versus Endotracheal Tube Alone on First-attempt Intubation Success in Prehospital Emergency Intubation (BETA Trial)

Condition: Acute Respiratory Failure Requiring Intubation  ·  Sponsor: Nantes University Hospital

PhaseNA
Planned participants710
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Emergency intubation is routinely performed in the prehospital setting. Airway management in the prehospital setting has substantial challenges, such as hostile environment or lack of technical support in case of first attempt intubation failure, and inherent risk of complications, such as hypoxemia, aspiration or oesophageal intubation. This risk is higher when several attempts are needed to succeed endotracheal intubation. Thus, a successful first attempt intubation is highly desirable to avoid adverse intubation-related events. Noteworthy, prehospital emergency intubation is associated with a lower rate of first attempt intubation success when compared to emergency intubation in the emergency department (ED). Research is needed to overcome the specific challenges of airway management in the prehospital setting, and to improve the safety and efficiency of prehospital emergency intubation. Literature reports that the use of assistive devices such as bougie may increase the rate of first-attempt intubation success in the ED. To date, no randomized trial has ever studied this device in the prehospital setting. Thus, the aim of the BETA trial is to compare first attempt intubation success facilitated by the bougie versus the endotracheal tube alone in the prehospital setting.

This description comes directly from the study's public registry record.

Talk to the study team

Quentin LE BASTARD, MD  ·  0240087839  ·  quentin.lebastard@chu-nantes.fr

Always discuss trial participation with your own doctor first.

Locations (10)

Nantes University HospitalNantes, Loire Atlantique, FranceRecruiting
CHU de BesançonBesançon, FranceRecruiting
CHU de BordeauxBordeaux, FranceRecruiting
CHU de Clermont-FerrandClermont-Ferrand, FranceRecruiting
CHD La Roche sur YonLa Roche-sur-Yon, FranceRecruiting
CH de LorientLorient, FranceNot Yet Recruiting
CHU de LyonLyon, FranceNot Yet Recruiting
CHU de NancyNancy, FranceRecruiting
CHU de PoitiersPoitiers, FranceRecruiting
CHU de RennesRennes, FranceRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06307392