Clinical trial Recruiting at 1 site Observational Ages 18 and up

Can large language models interpret parasternal block ultrasound images

Official title: Diagnostic Accuracy of Multimodal Large Language Models in Interpreting Ultrasound Images of Parasternal Intercostal Plane Blocks: A Prospective Observational Study

Run by Kanuni Sultan Suleyman Training and Research Hospital · NCT07915206 · Data updated 2026-11-12

This study tests whether multimodal language models can read ultrasound clips from parasternal intercostal plane blocks and match expert anesthesia assessments in adults undergoing elective surgery.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment32 (estimated)
SponsorKanuni Sultan Suleyman Training and Research Hospital
Academic / other
Locations1 site (Istanbul)
StatusRecruiting
StartedNovember 2, 2026
Main results expectedApril 2, 2027
Study endsApril 3, 2027
Registry record updatedNovember 6, 2026
Trial IDNCT07915206 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–85 years with ASA I–III undergoing elective surgery and receiving ultrasound-guided parasternal intercostal plane blocks, with complete ultrasound video recording.

Probably not a fit

Patients with poor-quality ultrasound recordings or those whose blocks are not interpretable by the AI may not receive any added benefit.

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

What this trial studies

This prospective observational study will compare multimodal large language models’ interpretations of ultrasound recordings from superficial and deep parasternal intercostal plane blocks with expert anesthesiologist assessments. Ultrasound videos of the injection and local anesthetic spread will be analyzed by models such as ChatGPT and Gemini using standardized prompts. The goal is to see if these models can correctly identify anatomical structures, assess injectate spread, determine block success, and flag potential risks. By enrolling 32 adults (ASA I–III) undergoing elective surgery, the study will evaluate diagnostic concordance between AI and human experts in a real clinical setting. No additional research procedures will be performed beyond routine anesthesia practice.

Why it matters

Potential benefit: If successful, AI-assisted ultrasound interpretation could support anesthesiologists by providing rapid, supplementary assessments during regional anesthesia.

How similar studies have gone: Previous work has explored AI-assisted image interpretation in anesthesia and ultrasound, with mixed but promising results for workflow support.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients aged 18-85 years.
* American Society of Anesthesiologists (ASA) physical status I-III.
* Undergoing elective surgery with an ultrasound-guided superficial or deep parasternal intercostal plane block.
* Complete ultrasound video recording of local anesthetic injection.
* Written informed consent for study participation.

Exclusion Criteria:

* Technical failure during block performance.
* Inadequate ultrasound recording quality preventing clear visualization of the needle tip or local anesthetic spread.
* Missing demographic data.
* Withdrawal of informed consent at any stage of the study.

Where it's running

  • Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital
    Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

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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.