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Breathing tube temperature may impact Kids' recovery after tonsil surgery

NCT ID NCT06838260

Knowledge-focused Sponsor: Bursa City Hospital 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether warming or cooling the breathing tube before placing it in children having tonsil surgery could reduce serious breathing complications like throat spasms or drops in oxygen. Researchers compared two groups of children to see if tube temperature made a difference. The goal was to find a simple way to make surgery safer for kids.

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

270 people

The number who actually took part.

Started

Mar 2025

Finished

Mar 2026

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

3 to 9 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: * Parents who agreed to participate in the study * Children undergoing adenotonsillectomy * ASA 1 and 2 class patients Exclusion Criteria: * Emergency surgery * Children with a history of difficult airway * Children who have had upper airway surgery * Presence or suspicion of upper or lower respiratory tract infection * History of cardiac and respiratory diseases * Patients with craniofacial malformations

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As listed by the trial registrant

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

Adenotonsillectomy

Contacts and locations

Locations

  • Bursa City Hospital

    Bursa, 16110, Turkey (Türkiye)

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