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New video mask may improve breathing tube placement in surgery

NCT ID NCT07361042

Knowledge-focused Sponsor: Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s. 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 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares a new video laryngeal mask with the classic version for helping patients breathe during general anesthesia. Researchers will measure how often the mask is placed correctly on the first try, how quickly it works, and any side effects. About 417 adults having planned surgery will take part.

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 417 people

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

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Sep 2027

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 * Patient without predicted difficult airway (MACOCHA score ≤ 2), undergoing a planned surgical procedure under general anesthesia with an indication for airway management using a laryngeal mask. * Patient aged 18 years or older. Exclusion Criteria * Patient younger than 18 years. * Patient with predicted difficult airway (MACOCHA score \> 2). * Patient with a history of difficult airway. * Patient requiring airway management with a method other than a laryngeal mask. * Refusal or failure to sign the informed consent for study participation. • Patient undergoing emergency surgery. * Administration of muscle relaxants for LMA insertion. * State Entropy value below 30 during LMA insertion. * State Entropy value above 60 during LMA insertion.

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As listed by the trial registrant

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

Supraglottic airway

How to take part

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  1. The official record

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