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New study tests video laryngeal mask against standard intubation

NCT ID NCT07365449

Knowledge-focused Sponsor: Akdeniz University Source: ClinicalTrials.gov ↗

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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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at two different ways to help patients breathe during surgery under general anesthesia. It compared a newer video laryngeal mask (SaCoVLM) with the traditional direct laryngoscopy method. Researchers measured blood pressure changes and how often the breathing tube was placed correctly on the first try in 204 adults having elective surgery.

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Study facts

What this study's own registry entry says, in plain language.

Participants

204 people

The number who actually took part.

Started

Mar 2025

Finished

Dec 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

This study included adult patients (≥18 years old) scheduled for elective surgery under general anesthesia at Akdeniz University Hospital between March and June 2024. Both male and female patients were eligible. Patients with known hypersensitivity to anesthetic agents, pregnant patients, those with gastroesophageal reflux disease, or active upper respiratory tract infections were excluded. A total of 204 patients were enrolled.

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: Age ≥ 18 years Scheduled for elective surgery under general anesthesia Requires tracheal intubation as part of the planned anesthetic technique American Society of Anesthesiologists (ASA) physical status I-III Able to provide written informed consent Exclusion Criteria: Age \< 18 years Pregnancy Known or suspected hypersensitivity to anesthetic agents used in the protocol History of gastroesophageal reflux disease or increased risk of aspiration Active upper respiratory tract infection Predicted difficult airway (Mallampati class IV, mouth opening \< 3 cm, limited neck mobility) Severe cardiopulmonary instability Emergency surgery Upper airway pathology (airway trauma, tumor, edema, infection) Coagulopathy or bleeding tendency Inability to cooperate or provide informed consent

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As listed by the trial registrant

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

Airway management

Contacts and locations

Locations

  • Akdeniz University Hospital

    Antalya, Please Select:, 07050, Turkey (Türkiye)

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