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Which airway device wins for kids? new study compares i-Gel and Air-Q

NCT ID NCT07141498

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at two different breathing devices (i-Gel and Air-Q) used in children aged 1 to 8 during planned surgeries. Doctors checked how well each device fit using a tiny camera and measured how much air got into the stomach using ultrasound. The goal was to see which device works better and causes fewer side effects like sore throat.

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

91 people

The number who actually took part.

Started

Aug 2025

Finished

Jan 2026

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

Children aged 1-8 years (ASA I-III) undergoing elective pediatric surgery under general anesthesia at Ankara Bilkent City Hospital. Eligible participants will require supraglottic airway device placement (i-Gel or Air-Q sp3G).

Ages

1 year to 8 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: * Age 1-8 years * ASA I-III * Elective pediatric or urological surgery under general anesthesia with SGA use * Informed consent obtained from parents/guardians Exclusion Criteria: * Parental refusal or inability to consent * ASA \> III * Recent or current upper respiratory tract infection * History of difficult airway * Increased aspiration risk * Urgent/emergency surgery or non-fasted patients * Known allergy or contraindication to anesthetic agents * Severe asthma (attack within last 6 months) * Structural airway anomalies * Gastrointestinal pathology affecting stomach emptying * Previous stomach surgery

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Ankara Bilkent City Hospital, Department Of Anesthesiology and Reanimation

    Ankara, Turkey (Türkiye)

More trials for these conditions

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