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Can a simple breathing adjustment make anesthesia recovery safer for kids?

NCT ID NCT07323420

Knowledge-focused Sponsor: Kırıkkale University 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Sep 10, 2026 · Updated 3 times

Summary

This study looks at two different breathing settings (1:2 vs. 1:3 inspiratory-to-expiratory ratio) used during anesthesia in children aged 2-12 having dental procedures. Researchers will measure vital signs, breathing quality, and recovery to see which setting leads to smoother emergence from anesthesia. The goal is to find the safest way to help children breathe on their own again after the procedure.

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

75 people

The number who actually took part.

Started

Apr 2026

Finished

Aug 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 will include pediatric patients aged 2 to 12 years who are scheduled to undergo routine dental procedures under general anesthesia at our faculty. Eligible participants are classified as American Society of Anesthesiologists (ASA) Physical Status I or II. Patients with airway anomalies, significant adenoid hypertrophy, macroglossia, retrognathia, severe obesity, developmental delays, or a history of delayed emergence from anesthesia will be excluded. Children requiring anesthesia for less than 1 hour or more than 3 hours, those with known pulmonary or airway diseases, neuromuscular disorders affecting respiration, or receiving medications that could alter spontaneous breathing during emergence (e.g., atropine, lidocaine, steroids) are also excluded. Written informed consent must be obtained from parents or legal guardians prior to participation.

Ages

2 to 12 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: * Pediatric patients scheduled for dental procedures under general anesthesia at our faculty. * American Society of Anesthesiologists (ASA) Physical Status I or II. * Age between 2 and 12 years. * Written informed consent obtained from parents or legal guardians. Exclusion Criteria: * Patients whose parents or legal guardians decline participation. * Presence of adenoid hypertrophy \>30%. * Macroglossia or retrognathia. * Severe obesity or developmental delay. * History of delayed emergence from anesthesia. * ASA Physical Status III or higher. * Anesthesia duration less than 1 hour or more than 3 hours. * Patients with difficult airway management or ventilation. * Known pulmonary or airway diseases or anomalies. * Use of pharmacological agents that may affect spontaneous respiratory quality. * Presence of neuromuscular disorders affecting respiratory function. * Age \<2 years or \>12 years. * Administration of medications intraoperatively or preoperatively that may influence respiratory dynamics during emergence (e.g., atropine, lidocaine, steroids).

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Conditions

The condition(s) this trial relates to.

Respiratory Aspiration

As listed by the trial registrant

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

General anesthesia Pediatric anesthesia Respiratory function

Contacts and locations

Locations

  • Kırıkkale University, Faculty of Dentistry

    Kirikkale, Turkey (Türkiye)

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