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Interventional AI-Human Collaboration for Steatotic Liver Disease Screening

23 maggio 2026 aggiornato da: Yu Shi, Shengjing Hospital

AI-Driven Opportunistic Screening and Risk-Adapted Management of Steatotic Liver Disease

Steatotic liver disease (SLD) is one of the most prevalent chronic liver diseases worldwide, affecting nearly 30% of the global population and projected to exceed 55% by 2040. Timely identification and management of intermediate- and high-risk SLD patients are essential, yet early detection remains challenging because current diagnostic modalities, such as biopsy, ultrasonography, and serum indices, are invasive, insensitive, operator-dependent, or difficult to scale. In contrast, non-contrast CT is widely available in routine care and offers substantial potential for opportunistic SLD screening, although this value has not been fully utilized. Our previously developed MAOSS model accurately identifies intermediate- and high-risk individuals, with MAOSS score≥1.6 combined with Fibro Score ≥1.7, demonstrating high sensitivity and specificity in our large-scale retrospective study. However, despite these promising retrospective findings, the model has not undergone prospective interventional validation, and it remains unclear whether an AI-guided workflow can truly enhance clinical risk stratification, diagnostic yield, and downstream management in real-world SLD populations. Therefore, a prospective intervention study is needed to determine whether MAOSS-guided identification and recall of at-risk individuals can meaningfully improve fibrosis detection and optimize clinical care pathways for SLD.

Panoramica dello studio

Descrizione dettagliata

The AIG-SLD Screening Project is a single-arm, open-label, prospective interventional study designed to evaluate the effectiveness of a MAOSS-guided identification and AI-human collaboration recall strategy for detecting individuals at intermediate or high risk of steatotic liver disease (SLD) and for assessing intervention outcomes. The trail will prospectively and consecutively enroll around 8000 eligible adults aged ≥18 years who undergo routine chest or abdominal non-contrast CT (NCCT) with adequate hepatic coverage .

The AI system i.e. MAOSS will be embedded within the standard clinical workflow to evaluate the real-world performance and the impact of AIG-SLD screening. All eligible NCCT scans will be evaluated through two parallel streams:

  1. Standard of Care (SoC) workflow: Radiologists perform independent assessments, first-line radiologists review followed by a senior radiologist finalizing the report.
  2. AIG workflow: The MAOSS system simultaneously analyzes the identical imaging data in real-time.

The system screens patients with clinically suspected SLD by flagging those with a MAOSS score ≥1.6 and a FIBRO Score ≥1.7 for recall. These algorithmic flags will be compared against radiologists' determinations of clinically significant SLD. Management pathways are defined as follows: (1) Concordant cases: If the Standard of Care (SoC) and the AIG pathway agree (both recommending recall or both recommending no recall), the agreed-upon decision will be executed. (2) Discordant cases: If the SoC and AIG pathways disagree, patients will be recalled for primary hepatology care to ensure safety.

Primary hepatology care begins with the collection of questionnaires regarding medical history, lifestyle, alcohol consumption, and metabolic risks (Type 2 Diabetes Mellitus, obesity, metabolic syndrome, significant alcohol consumption, or viral hepatitis) followed by further serum laboratory tests and Transient Elastography (e.g., FibroScan). Recalled patients will be managed according to the MAOSS pathway starting with FIB-4 stratification (<1.3, 1.3-2.67, >2.67), followed by FAST stratification (<0.35, ≥0.35) as needed. Intermediate-to-high-risk patients will proceed to escalated care involving MRE, MRI-PDFF, or liver biopsy. Management is then determined by MRE-derived Liver Stiffness Measurement (LSM): patients with LSM < 3.5 kPa will receive lifestyle interventions and annual reassessment; those with LSM 3.5-5.0 kPa (F2-F3) will receive pharmacological or therapeutic interventions; and those with LSM ≥ 5.0 kPa (F4) will undergo cirrhosis-based management. Patients in the latter two groups will be reassessed every six months to monitor changes in steatosis and fibrosis.

Tipo di studio

Interventistico

Iscrizione (Stimato)

7969

Fase

  • Non applicabile

Contatti e Sedi

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

Luoghi di studio

    • Liaoning
      • Shenyang, Liaoning, Cina, 110004
        • Shengjing Hospital of China Medical University

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

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

  • Adults aged ≥18 years undergoing routine non-contrast or contrast-enhanced chest or abdominal CT examination.
  • CT images with adequate hepatic coverage and sufficient image quality for MAOSS analysis.
  • Willing to undergo the recall evaluation and either: having a FIB-4 result within the past 1 month, or willing to complete blood testing (ALT, AST, platelet count) required for FIB-4 calculation and undergo FibroScan or MRE assessment.
  • Willing to participate in the study and able to provide written informed consent at the time of recall.

Exclusion Criteria:

  • Known malignant liver tumors (e.g., HCC, cholangiocarcinoma) or a history of liver transplantation or major hepatic resection.
  • Known cirrhosis based on noninvasive fibrosis assessment tests, liver biopsy or complications of decompensated disease, or with a documented history of cirrhosis identified by clinical notes will be excluded.
  • Biliary obstruction, acute cholangitis, or other conditions that may interfere with interpretation of liver biochemistry or fibrosis risk assessment.
  • CT images with severe artifacts or incomplete liver coverage preventing reliable MAOSS analysis.
  • Severe acute systemic illness (e.g., sepsis, shock, acute heart failure), or pregnancy or breastfeeding.
  • Unwilling or unable to complete recall procedures, including required blood tests, FibroScan, or MRE when indicated, or unable to comply with study follow-up.
  • Severe comorbidity with an expected survival of less than 1 year (e.g., terminal malignancy).

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

  • Scopo principale: Selezione
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: AI-human collaboration for SLD screening
In the prospective analysis phase, all eligible NCCT scans will be evaluated through two parallel streams: 1. Standard of Care (SoC) workflow: Radiologists perform independent assessments as per standard clinical procedures (e.g., first-line radiologists' reviews followed by senior radiologist finalizing the report). 2. AIG workflow: The MAOSS system simultaneously analyzes the identical imaging data in real-time.
The system screens patients with clinically suspected SLD by flagging those with a MAOSS score ≥1.6 and a FIBRO Score ≥1.7 for recall. These algorithmic flags will be compared against radiologists' determinations of clinically significant SLD. Management pathways are defined as follows: (1) Concordant cases: If the Standard of Care (SoC) and the AIG pathway agree (both recommending recall or both recommending no recall), the agreed-upon decision will be executed. (2) Discordant cases: If the SoC and AIG pathways disagree, patients will be recalled for primary hepatology care to ensure safety and avoid potential missed diagnosis.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Effective referral yield for escalated hepatology care
Lasso di tempo: 6 months
Effective referral yield: the proportion of patients referred for escalated hepatology care confirmed with clinically significant (or above) fibrosis by MRE/liver biposy. A non-inferiority test (and estimates of the associated absolute and relative differences) will be performed for effective referral yield between SoC and AIG workflow.
6 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Real-World Screening Specificity
Lasso di tempo: Duration of the study (12 months)
A critical safety endpoint is to determine if AIG-SLD care pathway maintains a high specificity to prevent false referral, thereby avoiding unnecessary interventions.
Duration of the study (12 months)
Real-World Screening Sensitivity
Lasso di tempo: Duration of the study (12 months)
A critical efficacy endpoint is to determine if AIG-SLD care pathway is sufficiently sensitive to identify patients who actually need interventions.
Duration of the study (12 months)
Real-World Screening Negative predictive value
Lasso di tempo: Duration of the study (12 months)
This evaluates the AIG-SLD care pathway's ability to correctly exclude low-risk patients who actually do not need interventions.
Duration of the study (12 months)
Intervention Success (Fibrosis Reversion)
Lasso di tempo: Duration of the study (12 months)
The proportion of patients referred for escalated care achieves fibrosis stage reversion.
Duration of the study (12 months)
Intervention Success (Steatosis Reversion)
Lasso di tempo: Duration of the study (12 months)
The proportion of patients referred for escalated care achieves steatosis stage Reversion.
Duration of the study (12 months)
Quantitative Liver Stiffness Trends
Lasso di tempo: Duration of the study (12 months)
The overall longitudinal changes in Liver Stiffness Measurement (LSM) values for all patients referred to escalated care.
Duration of the study (12 months)
Quantitative Liver Steatosis Trends
Lasso di tempo: Duration of the study (12 months)
The overall longitudinal changes in Liver Fat Content (CAP/PDFF) values for all patients referred to escalated care.
Duration of the study (12 months)
Intervention Patient Adherence
Lasso di tempo: Duration of the study (12 months)
The overall intervention adherence rate for all patients referred to escalated care.
Duration of the study (12 months)

Collaboratori e investigatori

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Pubblicazioni e link utili

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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 (Effettivo)

24 febbraio 2026

Completamento primario (Stimato)

30 agosto 2026

Completamento dello studio (Stimato)

24 febbraio 2027

Date di iscrizione allo studio

Primo inviato

23 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

23 maggio 2026

Primo Inserito (Effettivo)

29 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

29 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

23 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO

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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