Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

AI boosts radiologist speed in reading chest scans

NCT ID NCT07640906

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looks at whether an AI tool can help radiologists (doctors who read chest CT scans) write their reports faster without sacrificing quality. About 75 radiologists from several hospitals will use the AI as part of their normal work. Researchers will compare report time and quality before and after the AI tool is introduced.

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 75 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 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.

Who is studied

The study population is defined as follows: 1. Radiologists: Attending radiologists who routinely interpret chest CT scans as part of their clinical duties at the participating medical centers. 2. Chest CT Scans: Clinically indicated, non-contrast chest CT examinations acquired from the patient populations served by the participating centers. The scans are stratified into two groups based on the date of acquisition: before and after the implementation of the AI reporting system.

Ages

18 years and older

Sex

Anyone

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.

The study participants include both the radiologists whose performance is evaluated and the chest CT scans they interpret. Eligibility criteria are defined for both. 1\. Inclusion Criteria 1.1 For Radiologists 1. Board-certified radiologists specializing in or routinely performing thoracic imaging. 2. Employed at one of the participating study centers for the entire duration of both the without-AI and with-AI study periods. 3. Interpreted a minimum of eligible chest CT scans (e.g., \> 50 scans) during both the without-AI and with-AI data collection periods. 1.2 For Chest CT Scans 1. Non-contrast chest CT examinations performed for any clinical indication. 2. Scans completed and finalized during the defined with-AI or without-AI study periods. 3. Patient age 18 years or older at the time of the scan. 2\. Exclusion Criteria 2.1 For Radiologists: 1. Radiologists who joined, left, or were on extended leave (e.g., \>4 weeks) from the participating center between the with-AI and without-AI study periods. 2. Radiologists who interpreted fewer than the minimum required number of eligible scans in either study period. 3. Radiologists who voluntarily decline to have their de-identified performance data included in the study analysis. 4. Radiologists who decline to provide demographic or occupational information (e.g., years of professional experience or sex)-variables that may serve as potential confounders-will be excluded from adjusted and stratified analyses that require such covariates. 2.2 For Chest CT Scans 1. CT scans of pediatric patients (age \< 18 years). 2. Contrast-enhanced chest CT studies. 3. Studies performed for specific procedural guidance (e.g., biopsy, ablation). 4. Studies deemed technically inadequate for primary interpretation by radiologist (e.g., severe motion artifact, incomplete study). 5. Studies for which the AI system fails to generate a valid preliminary report draft. This includes possible system failures, algorithm errors, or cases where the generated draft is deemed technically unusable (e.g., empty, garbled, or based on critically flawed image analysis). 6. The lack of relevant information (diagnosis, clinical scenario, etc.). Chest CT data will be excluded from corresponding analyses if the required information, which is necessary for confounding control, subgroup analyses, or other pre-specified analyses, is unavailable. Such scenarios include data that cannot be retrospectively retrieved, incompletely recorded, or restricted due to ethical or institutional requirements.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Artificial intelligence (AI) in diagnosis are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

Thoracic Diseases

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

    2 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

  • Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai

    Shanghai, China

  • United Imaging Intelligence, Shanghai, Shanghai

    Shanghai, China

More trials for these conditions

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