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Which video laryngoscope works best when the neck Can't move?

NCT ID NCT07802522

Knowledge-focused Sponsor: Uniwersytet Radomski im. Kazimierza Pułaskiego Source: ClinicalTrials.gov ↗

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time

Summary

This trial tests four different videolaryngoscopes, including the VisionPro, to see which one performs best when inserting a breathing tube in patients whose neck is immobilized with a cervical collar. The study includes 200 adults undergoing laparoscopic surgery, all with a collar in place to simulate a neck injury. Researchers will measure how often the tube is placed successfully on the first try and how long the procedure takes. The goal is to find the most reliable device for difficult airway situations.

What this could mean

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

Active substance
VisionPro hyperangulated videolaryngoscope, a device used for tracheal intubation
What this could lead to
If the VisionPro performs well, it could become a preferred tool for safely intubating patients with cervical spine injuries, potentially reducing complications.
What could go wrong
This is a single-center trial with 200 patients, so results may not apply broadly. The study compares devices, not patient outcomes, and success depends on operator skill.

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 200 people

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

Started

Aug 2026

Expected to finish

Oct 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

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.

Inclusion Criteria: * ASA status 1-3 * aged over 18 years old * male and female * laparoscopic surgery Exclusion Criteria: * known difficult laryngoscopy * difficult face mask ventilation * aged under 18 years old * previous history of awake tracheal intubation * patients with BMI \> 30 kg m-2

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As listed by the trial registrant

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

Airway management Cervical spine immobilisation Difficult airway

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

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Uniwersytet Radomski

    Radom, Masovian Voivodeship, 26-600, Poland

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