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Which video laryngoscope wins the race to place a breathing tube?

NCT ID NCT07577648

Knowledge-focused Sponsor: University of Malaya 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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 two types of video laryngoscopes (Astra-Vue and C-MAC D-Blade) to see which one helps doctors place a breathing tube faster and more easily in adults having surgery under general anesthesia. About 60 adults aged 18 to 70 will take part. The main goal is to measure the total time needed to insert the tube, along with success rates and any complications.

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 60 people

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

Started

Dec 2025

Expected to finish

May 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 to 75 years

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: * Adult patients aged 18 to 70 years old requiring endotracheal intubation for elective or semi-emergency surgery under general anaesthesia * ASA I, II and stable ASA III patients * Patient with Mallampati Score Grade 1 to 3 Exclusion Criteria: * Patients with known airway abnormalities or anticipated difficult intubation, * Patients with desaturation before intubation, * Patients with high risk for aspiration requiring rapid sequence induction * Patient with known cervical pathology. * Patient refuse to participate

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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

  • Universiti Malaya Medical Centre

    Petaling Jaya, Kuala Lumpur, 59100, Malaysia

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