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Gentler breathing tube may speed recovery for Kids' hernia surgery

NCT ID NCT07511764

Knowledge-focused Sponsor: Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 ways to help children breathe during laparoscopic hernia repair: a traditional breathing tube (endotracheal intubation) and a less invasive mask (laryngeal mask airway). Researchers will enroll 266 children aged 1-10 to see which method is safer and leads to faster recovery. The goal is to find the best approach for this common surgery.

What this could mean

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

Active substance
General anesthesia with either laryngeal mask airway (LMA) or endotracheal intubation (ETT)
What this could lead to
If LMA proves as safe as ETT, it could become the preferred airway method for this common childhood surgery, leading to faster recovery and fewer complications.
What could go wrong
This is a relatively small, early-stage study (266 children) comparing two established techniques. Results may not apply to all children or surgeries, and LMA might not be safe in all cases.

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 266 people

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

Started

Dec 2025

Expected to finish

Sep 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

1 year to 10 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: * being between 1 and 10 years of age, * having a planned laparoscopic inguinal hernia repair, * being classified as ASA I-II, * having given informed consent from the parent. Exclusion Criteria: * Obesity (body weight \>95th percentile), * symptomatic gastroesophageal reflux, * high risk of aspiration, * upper airway anomalies, * history of difficult intubation, * acute respiratory tract infection, * emergency surgical indication, * need for conversion from laparoscopy to open surgery, * presence of additional systemic risks such as immunodeficiency/malignancy.

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Conditions

The condition(s) this trial relates to.

Hernia, Inguinal

As listed by the trial registrant

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

Inguinal hernia repair

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Dicle University

    RECRUITING

    Diyarbakır, Eyalet/Yerleşke, 21070, Turkey (Türkiye)

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