임상 레이더 AI
임상시험 NCT07430501 (ARTEMIS)은(는) 대사 기능 장애 관련 지방간 질환에 대해 대상자모집전 상태입니다. 모든 세부 정보를 보려면 임상시험 레이더 카드 뷰와 AI 발견 도구를 확인하거나 여기에서 무엇이든 물어보세요.
하나의 임상시험이 필터 기준과 일치합니다.
카드 뷰

Using Digital Twin Technology and Clinical Decision Support Systems to Improve the Early Detection, Personalised Treatment, and Long-term Monitoring of Patients Across the Full Spectrum of Metabolic-associated Fatty Liver Disease (MAFLD). (ARTEMIS) 7,720 관찰 연구 비대면

대상자모집전
임상시험 세부 정보는 주로 영어로 제공됩니다. 하지만 임상 레이더 AI가 도와드릴 수 있습니다! '임상시험 설명'를 클릭하여 선택한 언어로 임상시험 정보를 확인하고, 이에 대해 AI와 논의해 보세요.
임상시험 NCT07430501 (ARTEMIS)은(는) 대사 기능 장애 관련 지방간 질환에 대해 알아보는 관찰연구입니다. 현재 상태는 대상자모집전이며, 2026년 2월 23일부터 참여 신청이 가능합니다. 7,720명의 참여자를 모집할 예정입니다. Hospital Universitari Vall d'Hebron Research Institute이(가) 진행하는 이 연구는 2027년 9월 2일까지 진행될 예정입니다. ClinicalTrials.gov의 가장 최근 정보는 2026년 2월 24일에 갱신되었습니다.
간단한 개요
The goal of this observational study is to create a detailed virtual model to better understand how Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) develops. This model will also help predict heart problem at different stage of the disease.
상세한 설명
  1. - Glossary CT : Computed Tomography CVD : Cardio-Vascular Disease HCC : Hepato Cellular Carcinoma MASH : Metabolic dysfunction-associated steatohepatitis MASLD : Metabolic dysfunction-Associated Steatotic Liver Disease MRI : Magnetic Resonance Imaging PET : Positron Emission Tomography SLD : Steatotic Liver Disease TACE : Trans-Arterial ChemoEmbolisation TARE : Trans-Arterial RadioEmbolisation TIPS : Transjugular...
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공식 제목

AcceleRating the Translation of Virtual Twins Towards a pErsonalised Management of Steatotic Liver Patients

질환명
대사 기능 장애 관련 지방간 질환
출판물
이 임상시험에 대해 발표된 과학 논문 및 연구 자료.
기타 연구 식별자
  • ARTEMIS
  • ARTEMIS_HE-HLTH2023
  • 101136299 (기타 보조금/자금 번호) (Horizon Europe | RIA (Topic HORIZON-HLTH-2023-TOOL-05-03))
NCT 번호
실제 연구 시작일
2026-02-23
최신 업데이트 게시
2026-02-24
예상 연구 완료일
2027-09-02
계획된 등록 인원
7,720
연구종류
관찰연구
상태
대상자모집전
키워드
MASLD
Virtual twins
fatty liver patients
시험군 / 개입
참가자 그룹/시험군개입/치료
ARTEMIs cohort
* Clinical Use Case #1\& 2: Adult patients diagnosed with MASLD/MASH. Clinical Use Case #2, subgroup of patients with cardiovascular disease: Adult patients diagnosed with cardiac fibrosis, with or without MASLD. * Clinical Use Case #3: Adult patients diagnosed with cirrhosis. * Clinical Use Case #4: Adult patients diagnosed with HCC. * Control group: Adult patients with neither liver conditions nor cardiovascular ev...더 보기
Data recollection
Only data recollection for their use in the training, testing and early validation of computational models (but no other intervention) will be performed.
주요결과변수
결과변수측정값 설명시간 범위
Liver disease progression and regression in MASLD patients
Probability rates of liver disease progression or regression in MASLD patients, including fibrosis stage changes and development of steatohepatitis (MASH), assessed using validated non-invasive tests, imaging techniques, and liver histology when available
From baseline assessment to last available follow-up (minimum 1 year, up to 5 years)
이차결과변수
결과변수측정값 설명시간 범위
Incidence of cardiovascular events in MASLD patients
Occurrence of cardiovascular events including myocardial infarction, stroke, atrial fibrillation, and heart failure in MASLD patients during retrospective follow-up.
Up to 5 years after baseline assessment
참여 도우미
적격성 기준

연령대
성인, 노인
최소 연령
18 Years
참여 가능한 성별
전체
건강한 참가자 허용
  1. - Clinical Use Case 1: Liver disease staging in MASLD patients - Prediction model of fibrosis changes (progression and regression), with ability to distinguish between fast and non-fast fibrosis progression among MASLD patients.

    • Age ≥18 years
    • Diagnosis of MASLD confirmed by radiological imaging (any type: MR, CT, PET, VCTE, US, USE...) or histology (gold standard, following MASH SAF score)
    • With at least one follow-up of minimum 1 year after diagnosis of MASLD, with radiological imaging or histology
  2. - Clinical Use case 2: MASLD and progression of cardiovascular diseases

    • Age ≥18 years MASLD patients regardless of disease stage of severity (from simple steatosis to cirrhosis)
    • Patients without known heart disease
    • Cardiovascular assessment available

3.1- Clinical Use case 3-TIPS: Patients with cirrhosis and portal hypertension who receive TIPS placement.

  • Age ≥18 years
  • TIPS indication (Baveno VII), except pre-emptive and salvage TIPS.
  • Recurrent variceal bleeding after failure of the usual pharmacological and endoscopic methods
  • Refractory or recurrent ascites or difficult to treat
  • Refractory Hydrothorax
  • Patients with diagnosis of liver cirrhosis (based on laboratory parameters, clinical, endoscopic, radiological or histological findings), of any aetiology.

3.2.- Clinical Use Case 3-LT: Patients with cirrhosis and portal hypertension who received liver transplantation.

  • Age ≥18 years

  • All patients with cirrhosis (all aetiologies) who were transplanted

    4.- Clinical Use Case 4: Prediction of cardiac complications due to HCC treatments* (*Note: includes surgical interventions, ablation, TACE, TARE, SIRT and immunotherapies)

  • Age ≥18 years

  • Diagnosis of HCC (any aetiology)

  • Cross sectional imaging follow-up (any modality) of liver diseases 6 months after treatment

  • Non-cirrhotic or no more than Child-Pugh B cirrhosis.

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

  • Patients without history of prior HCC

  • Patients with a history of hypertension should be well controlled (< 140/90 mmHg) on a regimen of antihypertensive therapy.

  • With a minimum follow-up of two years or until death, after diagnosis of HCC

    5.- Other populations (participation in control arms)

  • Age ≥18 years

  • Subjects presenting cardiac fibrosis, without a known MASLD diagnosis (as controls for use case 2)

  1. - Clinical Use Case 1: Liver disease staging in MASLD patients - Prediction model of fibrosis changes (progression and regression), with ability to distinguish between fast and non-fast fibrosis progression among MASLD patients.

    • Missing data on blood glucose, BMI and metabolic status.
    • Patients who have received systemic chemotherapy
    • Patients with hepatitis B (HBV) and hepatitis C (HCV), alcoholic liver disease (more than 5 years of drinking history, equivalent to alcohol volume ≥ 30g / D in male and ≥ 20g / D in female), drug-induced liver disease or autoimmune hepatitis.
    • Subjects having a significant risk of bleeding (platelet < 50x109 / L, prothrombin activity < 50%)
    • Presence of any other form of chronic liver, at the time of MASLD diagnosis.
  2. - Clinical Use case 2: MASLD and progression of cardiovascular diseases

    • Association with another cause of liver disease
    • History of hepatitis B or C
    • Already known coronary artery disease
    • History of cardiovascular events

3.1- Clinical Use case 3-TIPS: Patients with cirrhosis and portal hypertension who receive TIPS placement.

  • Non-cirrhosis TIPS
  • Portosinusoidal vascular disease
  • Complete portal vein thrombosis
  • Patients with surgical porto-caval shunts.
  • Patients with evidence of current locally advanced or metastatic malignancy
  • Patients with acute or chronic heart failure (New York Heart Association \[NYHA\]).
  • Patients with chronic obstructive pulmonary disease GOLD grade III/IV
  • Patients with chronic kidney disease requiring renal replacement therapy
  • Patients with a known infection with human immunodeficiency virus (HIV) or have clinical signs and symptoms consistent with current HIV infection
  • Patients with previous liver transplantation
  • Patients lost to follow-up and therefore have an incomplete 1-year follow-up

3.2.- Clinical Use Case 3-LT: Patients with cirrhosis and portal hypertension who received liver transplantation.

  • Patients who were transplanted due to acute liver failure.

  • Patients who were already transplanted before (retransplant)

  • Patients who are lost to follow-up in the first 5 years after liver transplant.

    4.- Clinical Use Case 4: Prediction of cardiac complications due to HCC treatments* (*Note: includes surgical interventions, ablation, TACE, TARE, SIRT and immunotherapies)

  • Mixed-tumor HCC based on radiological and/or pathological examination

  • Uncontrolled inter-current illness or psychiatric illness or social situations that would limit compliance with study requirements.

  • Subjects with history of another primary cancer

  • Fully recovered from any prior surgery and/or radiation and none within 2 weeks of initiating treatment.

  • Subjects with active hepatitis B or C on antiviral compounds may remain on such treatment, except for interferon.

  • Subjects with diagnosis of tumor of mixed origin, either from radiological or biopsy report.

    5.- Other populations (participation in control arms)

  • Patients with diagnosis of MASLD

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연구 대표 연락처
연락처: Jose Raul Herance, PhD, 937372444, [email protected]
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Barcelona

Vall d´Hebron Institute de Recerca (VHIR), Barcelona, Barcelona, 08035, Spain