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New breathing technique may cut lung risks in Kids' chest surgery

NCT ID NCT05386901

Knowledge-focused Sponsor: Jiaxiang Chen Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether a personalized breathing method during chest surgery could lower the chance of lung problems afterward in children under 5. Sixty-three kids having chest surgery were split into two groups: one got the standard breathing settings, the other got settings tailored to their lung stiffness. The goal was to see if the tailored approach reduced complications like cough, low oxygen, or pneumonia in the week after surgery.

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

63 people

The number who actually took part.

Started

Jun 2022

Finished

Oct 2024

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 month to 5 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: * Children undergoing elective thoracoscopic pulmonary surgery. * Written informed consent. * Children under 5 years old (including 5 years old) * ASA classification 1-2 * Respiratory Risk Assessment in Catalan Surgical Patients (ARISCAT) Criteria Low or Moderate Risk Exclusion Criteria: * Symptoms of upper respiratory tract infection or pulmonary infection in the past 4 weeks, chest X-ray suggests pneumonia * Severe circulatory disease * Children with bullae * Intraoperative arterial blood pressure monitoring cannot be performed * Respiratory Risk Assessment in Catalan Surgical Patients (ARISCAT) Criteria Rated High Risk

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As listed by the trial registrant

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

Anesthesia Surgery

Contacts and locations

Locations

  • Shenzhen Children's Hospital

    Shenzhen, Guangdong, 518038, China

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