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Evaluation of Large Language Models in Parasternal Block Ultrasound Interpretation

29 ottobre 2026 aggiornato da: Engin Ihsan Turan, Kanuni Sultan Suleyman Training and Research Hospital

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

This prospective observational study aims to evaluate the accuracy of multimodal large language models (LLMs) in interpreting ultrasound recordings of superficial and deep parasternal intercostal plane blocks.

Ultrasound recordings obtained during routine regional anesthesia procedures will be independently evaluated by LLMs using standardized prompts. Their ability to identify anatomical structures, assess local anesthetic spread, determine block success, and recognize potential procedural risks will be compared with expert anesthesiologist assessments.

The study aims to investigate the potential role of LLMs in ultrasound-guided regional anesthesia assessment and clinical decision support.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Descrizione dettagliata

Study Design and Participants This prospective observational study will evaluate the diagnostic accuracy of multimodal large language models (LLMs) in interpreting ultrasound recordings of superficial and deep parasternal intercostal plane blocks (S-PIP and D-PIP).

The study will include 32 adult patients aged 18-85 years, classified as American Society of Anesthesiologists (ASA) physical status I-III, undergoing elective surgery with an ultrasound-guided parasternal intercostal plane block.

Blocks will be performed by experienced anesthesiologists as part of routine clinical practice. Ultrasound recordings will include the local anesthetic injection and its spread within the targeted fascial plane. No additional procedures will be performed for research purposes.

Ultrasound Video Acquisition Ultrasound-guided S-PIP and D-PIP procedures will be recorded in video format, including the injection process.

Videos with inadequate visualization of relevant anatomical structures, needle placement, or local anesthetic spread will be excluded.

All recordings will be anonymized before evaluation. Each eligible recording will be assigned a unique identification code.

Large Language Model Evaluation ChatGPT (OpenAI) and Gemini (Google) will be evaluated using their latest available multimodal versions at the time of assessment. Exact model names, versions, access platforms, and evaluation dates will be documented.

The same ultrasound recording will be independently submitted to both models in MP4 format, provided that direct video analysis is supported by the selected model interfaces.

An identical standardized English-language prompt will be used for every recording and both LLMs. Each recording will be evaluated in a separate conversation to minimize contextual carryover.

Models will receive no patient-identifying information, expert interpretations, or feedback regarding the correctness of their responses.

The following eight questions will be presented in the same order:

  1. Identify the anatomical structures visible in this parasternal ultrasound recording.
  2. Based on the observed local anesthetic spread, determine whether the solution was deposited in the correct target fascial plane.
  3. Determine whether the local anesthetic spread is superficial or deep.
  4. If the observed spread is inadequate or occurs outside the target fascial plane, what corrective action would you recommend?
  5. Assess whether the needle tip is positioned within the appropriate fascial plane.
  6. Identify potential procedural risks involving adjacent structures, including the pericardium and internal mammary vessels.
  7. Which dermatomal levels are expected to be covered by this block?
  8. If the observed spread is inadequate or occurs outside the target fascial plane, would you recommend an additional injection? Models will be instructed to base their assessments exclusively on the provided ultrasound recording and to explicitly indicate when the available visual information is insufficient for a reliable conclusion.

Responses will be recorded without additional prompting or correction. Response time and other predefined performance parameters will also be documented.

Expert Assessment and Blinding Two experienced anesthesiology professors will participate in the expert assessment process. The first expert (Expert A) will independently review each ultrasound recording and answer the same eight standardized questions. These assessments will serve as the expert reference. LLM-generated responses and Expert A's responses will subsequently be anonymized and randomly coded to conceal their sources.

The second expert (Expert B), blinded to response origin, will independently evaluate the anonymized responses regarding their accuracy, clinical appropriateness, and agreement with the expert reference.

Responses will be assessed using predefined scoring criteria, including content similarity and an overall quality score ranging from 0 to 10.

Outcome Assessment The primary objective is to compare the diagnostic accuracy of ChatGPT and Gemini in identifying anatomical structures and determining whether the local anesthetic solution was correctly deposited within the intended fascial plane during parasternal intercostal plane blocks.

Secondary assessments will include classification of superficial versus deep local anesthetic spread, needle tip position, procedural risk identification, appropriateness of clinical recommendations, predicted dermatomal coverage, and agreement with expert assessments. Model response time, response quality, and reported confidence will also be evaluated.

Data Protection and Clinical Safety All recordings will be de-identified before submission to the LLM platforms. Model-generated interpretations will be used solely for research purposes and will not influence clinical decision-making or patient management.

The study will be conducted in accordance with the approved research protocol and applicable ethical and data protection requirements.

Tipo di studio

Osservativo

Iscrizione (Stimato)

32

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Engin ihsan Turan, principal investigator
  • Numero di telefono: +9005382431114
  • Email: enginihsan@hotmail.com

Luoghi di studio

      • Istanbul, Turchia (Türkiye), 34303
        • Health Science University İstanbul Kanuni Sultan Süleyman Education and Training Hospital

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione di probabilità

Popolazione di studio

32

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: COHORT
  • Prospettive temporali: PROSPECTIVE

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Patients Undergoing Parasternal Intercostal Plane Blocks

Adult patients undergoing ultrasound-guided superficial or deep parasternal intercostal plane blocks as part of routine clinical care. Anonymized ultrasound recordings of local anesthetic injection will be independently evaluated by ChatGPT and Gemini using identical standardized prompts. Model assessments will be compared with expert anesthesiologist evaluations.

Anonymized ultrasound recordings of parasternal intercostal plane blocks will be independently evaluated using the latest available multimodal versions of ChatGPT and Gemini. Both models will receive the same MP4 recordings and identical standardized prompts to assess anatomical structures, correct deposition of local anesthetic solution within the target fascial plane, injection spread, and potential procedural risks. Responses will be compared with expert anesthesiologist assessments. No AI-generated recommendations will influence patient care.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Correct Local Anesthetic Deposition
Lasso di tempo: During the ultrasound-guided block procedure

The accuracy of ChatGPT and Gemini in determining whether the local anesthetic solution was deposited within the intended fascial plane will be evaluated using ultrasound recordings. Model assessments will be compared with the expert reference assessment. Accuracy will be calculated as the percentage of correctly classified recordings.

During the ultrasound-guided block procedure

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Anatomical Identification Accuracy
Lasso di tempo: During the ultrasound-guided block procedure

The ability of ChatGPT and Gemini to correctly identify anatomical structures visible in parasternal intercostal plane block ultrasound recordings will be evaluated against expert anesthesiologist assessments. Anatomical identification performance will be scored using predefined criteria.

During the ultrasound-guided block procedure
Needle Tip Position
Lasso di tempo: During the ultrasound-guided block procedure

The accuracy of ChatGPT and Gemini in determining whether the needle tip is located within the intended fascial plane will be compared with the expert reference assessment. Results will be reported as the percentage of correctly classified recordings.

During the ultrasound-guided block procedure
Local Anesthetic Spread
Lasso di tempo: During the ultrasound-guided block procedure

The ability of each model to classify local anesthetic spread as superficial or deep and identify the observed spread pattern will be compared with expert assessments. Classification accuracy will be reported as a percentage.

During the ultrasound-guided block procedure
Procedural Risk Identification
Lasso di tempo: During the ultrasound-guided block procedure

The ability of each model to identify potential procedural risks involving adjacent anatomical structures, including the internal mammary vessels and pericardium, will be evaluated against expert assessments. Accuracy will be reported as the percentage of correctly classified recordings.

During the ultrasound-guided block procedure
Clinical Recommendation Quality
Lasso di tempo: During the ultrasound-guided block procedure

The appropriateness of recommendations regarding inadequate local anesthetic spread, corrective actions, and additional injection will be assessed by an independent expert anesthesiologist using a predefined scoring system ranging from 0 to 10, with higher scores indicating greater clinical appropriateness.

During the ultrasound-guided block procedure
Agreement With Expert Assessment
Lasso di tempo: During the ultrasound-guided block procedure

Agreement between ChatGPT, Gemini, and expert anesthesiologist assessments will be evaluated for predefined ultrasound interpretation parameters. Agreement will be quantified using Cohen's kappa for applicable categorical assessments.

During the ultrasound-guided block procedure

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

2 novembre 2026

Completamento primario (Stimato)

2 aprile 2027

Completamento dello studio (Stimato)

3 aprile 2027

Date di iscrizione allo studio

Primo inviato

29 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

29 ottobre 2026

Primo Inserito (Effettivo)

4 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

4 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 ottobre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • LLMs success-Parasternal Block

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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