Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New video mask could make anesthesia safer

NCT ID NCT07007403

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested a new third-generation video laryngeal mask in 50 adults undergoing general anesthesia. The goal was to see how often the mask worked on the first try, how quickly it provided good airflow, and if there were any side effects. The device uses a camera to help doctors place it correctly, potentially improving safety and speed during surgery.

What this could mean

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

Active substance
video laryngeal mask (device)
What this could lead to
If successful, this device could improve how doctors secure airways during surgery, making the process faster and safer.
What could go wrong
This is a small pilot study with only 50 participants, so results may not apply to everyone. The device might not work better than current methods.

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.

Participants

50 people

The number who actually took part.

Started

Jun 2025

Finished

Aug 2025

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.

Who is studied

Patients undergoing general anesthesia in the MNUL and Děčín Hospital.

Ages

10 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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Supraglottic airway are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Contacts and locations

Locations

  • Masarykova Nemocnice v Ústí nad Labem, Krajská Zdravotní a.s.

    Ústí nad Labem, Ústí nad Labem Region, 40001, Czechia

More trials for these conditions

Other studies related to the condition(s) this trial covers.