Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

AI-assisted chest CT report drafting to save radiologist time

Official title: An Evaluation Study of a Text-Based Chest CT-Assisted Diagnostic System: A Two-stage, Multicenter, Multireader Multicase (MRMC), Self-Crossover Controlled Trial

Run by Shanghai Zhongshan Hospital · NCT07634861 · Data updated 2026-11-12

This study tests whether an AI draft report can help experienced chest radiologists write chest CT reports faster without sacrificing quality.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorShanghai Zhongshan Hospital
Academic / other
Locations2 sites (Shanghai and 1 other locations)
StatusRecruiting
StartedJune 20, 2026
Main results expectedDecember 31, 2026
Study endsFebruary 15, 2027
Registry record updatedJune 9, 2026
Trial IDNCT07634861 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Board-certified radiologists with at least three years of post-certification experience in thoracic imaging and primary responsibility for chest CT reporting.

Probably not a fit

Radiologists without access to or familiarity with AI-assisted tools or those in workflows where AI drafting does not integrate well may not see benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicenter study evaluates an AI tool that generates preliminary chest CT report drafts to see if it can speed up report writing while preserving report quality. It uses a two-phase design: a retrospective crossover phase comparing AI-assisted and standard reporting on historical cases, followed by a prospective real-world phase where radiologists interpret new scans with AI support integrated into workflow. Outcomes include time saved per case and blinded quality assessments by senior physicians. The goal is to determine if the AI tool improves efficiency without compromising patient care.

Why it matters

Potential benefit: If successful, radiologists may produce faster reports with equal or better quality, potentially reducing turnaround times for chest CT diagnoses.

How similar studies have gone: Previous studies in similar MRMC designs have shown potential efficiency gains with AI-assisted reporting, though results vary by tool and setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Active board certification and ongoing routine clinical practice as an attending radiologist
* Independent institutional authority for chest CT image interpretation and final official diagnostic report issuance
* A minimum of three years of post-certification clinical experience in specialized thoracic imaging
* Legal and cognitive competence for study participation, with voluntary provision of written informed consent after full understanding of study purpose, procedures, risks and benefits

Exclusion Criteria:

* Direct participation in the development, training or validation of the trial's evaluated AI system
* Ongoing participation in concurrent studies with potential risks of interpretation bias, cognitive fatigue or study procedure interference (investigator-assessed)
* Any actual or perceived conflict of interest related to the evaluated AI system or its developers that may compromise objectivity in image interpretation and diagnostic reporting

Where it's running

  • Department of Radiology, Zhongshan Hospital, Fudan University
    Shanghai, China
    Recruiting
  • United Imaging Intelligence, Shanghai
    Shanghai, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.