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AI learns to read Children's breathing in the ER

NCT ID NCT07370623

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 is collecting data from 2,200 children aged 0 to 12 who come to emergency rooms with breathing problems. Researchers will use videos and clinical information to train an artificial intelligence system to automatically recognize different breathing patterns. The goal is to create a tool that helps doctors assess respiratory distress more objectively and quickly.

What this could mean

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

What this could lead to
If successful, this could lead to an AI tool that helps doctors quickly and objectively assess breathing problems in children, potentially improving emergency care.
What could go wrong
This is an early observational study focused on data collection and AI development, not a treatment trial. The AI system may not perform accurately enough for real-world use, and results may not apply to all hospitals.

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

About 2,200 people

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

Started

Oct 2025

Expected to finish

Dec 2027

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.

Who is studied

The study population consists of pediatric patients aged 0 to 12 years who visit the pediatric emergency departments of participating institutions. Clinical data, including basic demographic characteristics (e.g., sex, age, body weight, height), severity at presentation (e.g., KTAS level), vital signs, and emergency department management and outcomes (e.g., admission or discharge), as well as visual respiratory data, are collected during emergency care and used for the development and evaluation of a vision-language model-based system for automated assessment of pediatric respiratory patterns.

Ages

0 to 12 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: * Pediatric patients aged 0 to 12 years who present to participating pediatric emergency departments. * Patients for whom clinical data, including basic demographic characteristics (e.g., age, body weight), severity at presentation (e.g., KTAS level), vital signs, emergency department management and outcomes, as well as visual respiratory data, are available during emergency care. Exclusion Criteria: * Patients outside the specified age range. * Patients with insufficient or poor-quality clinical or visual respiratory data. * Patients whose data cannot be used due to withdrawal of consent or regulatory restrictions.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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

  1. The places running it

    3 sites. 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

  • Asan Medical Center, 88, Olympic-ro 43-gil, Songpa-gu

    RECRUITING

    Seoul, Seoul, 05505, South Korea

  • CHA Bundang Medical Center, CHA University, 9, Yatap-ro, Bundang-gu

    RECRUITING

    Seongnam-si, Gyeonggi-do, 13496, South Korea

  • Samsung Medical Center, 81, Irwon-ro, Gangnam-gu

    RECRUITING

    Seoul, Seoul, 06351, South Korea