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Could a single device make emergency intubation faster and safer?

NCT ID NCT07747922

Knowledge-focused Sponsor: Huseyin Cahit Halhalli, MD Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 05, 2026 · Last updated Sep 03, 2026 · Updated 3 times

Summary

This trial tests a new integrated tube-bougie prototype that combines the guidance of a bougie with an endotracheal tube into one device. Emergency medicine residents will use it, along with standard stylet and bougie techniques, on simulated normal and difficult airways. The goal is to see if the prototype reduces time to successful intubation and improves first-attempt success, which could lead to better airway management in emergencies.

What this could mean

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

Active substance
Integrated tube-bougie prototype (EPATS) - a device combining an elastic bougie with an endotracheal tube
What this could lead to
If successful, this prototype could offer a faster, more reliable intubation method, especially in emergency settings where videolaryngoscopy isn't available.
What could go wrong
This is a small simulation study with 40 participants, so results may not translate to real patients. The prototype is novel and may not outperform standard tools in practice.

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 40 people

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

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

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

Accepted

You do not need to have the condition being studied to take part.

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.

Inclusion Criteria: * Professional Status: Being an Emergency Medicine Resident actively undergoing specialty training at the University of Health Sciences, Kocaeli City Hospital, Department of Emergency Medicine. * Voluntary Participation: Voluntarily agreeing to participate in the study and providing written informed consent prior to enrollment. * Postgraduate year (PGY) 1-4 residents. * Willing and able to provide written informed consent. Exclusion Criteria: * Refusal to Participate: Declining to participate or refusing to provide written informed consent. * Physical or Neurological Limitations: Having any pre-existing physical, motor, or neurological impairment that could interfere with manual dexterity, procedural performance, or airway management simulation (e.g., hand injuries, tremors, etc.). * Inability to complete all study procedures.

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As listed by the trial registrant

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

Airway management Difficult airway Endotracheal 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

  • University of Health Sciences, Kocaeli City Hospital

    Köseköy, Kocaeli, 41060, Turkey (Türkiye)

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