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Which airway device is safer for kids? new study seeks answers

NCT ID NCT07252674

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jul 02, 2026 · Updated 4 times

Summary

This study watches 100 children aged 2-5 during surgery to compare two ways of helping them breathe: a laryngeal mask airway (a soft tube placed in the throat) and an endotracheal tube (a tube placed into the windpipe). Doctors will measure lung stress and watch for breathing problems after surgery. The goal is to learn which method might be gentler on young lungs.

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

100 people

The number who actually took part.

Started

Nov 2025

Finished

Jun 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

The study population consists of pediatric patients aged 2-5 years and weighing 10-20 kg who will undergo elective surgery under general anesthesia at Konya City Hospital. Participants will be classified as ASA physical status I-III. Patients who meet all inclusion criteria and do not meet any exclusion criteria will be included in the study.

Ages

2 to 5 years

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: * Children aged 2-5 years * Body weight between 10-20 kg * Patients classified as ASA physical status I-III * Elective surgery planned under general anesthesia Exclusion Criteria: * Presence of severe chronic lung disease (e.g., advanced bronchopulmonary dysplasia) * Uncontrolled or severe bronchial asthma * Severe cardiac failure (NYHA Class III-IV) * Diagnosis of pulmonary hypertension * History of major lung surgery * Severe obesity (BMI \> 95th percentile) * Children scheduled for abdominal or thoracic surgery * Procedures expected to last longer than two hours * Emergency surgeries * Children and/or parents who decline participation in the study

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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

  • Konya City Hospital

    Konya, Konya, Turkey (Türkiye)

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