Global Research Initiative for Patients Screening on MASH

NCT05651724 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2024-08-01

No results posted yet for this study

Summary

GRIPonMASH will assist (primary) health care providers clinicians to implement the latest patient care pathway, as described by the European Association for the Study of the Liver (EASL), to identify patients at risk of severe metabolic dysfunction-associated steatotic liver disease (MASLD) and to raise awareness. The primary objective is to implement a transmural patient care pathway, in order to identify patients with MASLD and its progressive form metabolic dysfunction-associated steatohepatitis (MASH) in primary care centres and clinics in 10 European countries.

Conditions

  • MASH
  • MASLD
  • MASH With Fibrosis
  • Fibrosis, Liver
  • Steatosis of Liver
  • Type 2 Diabetes
  • Obesity
  • Metabolic Syndrome
  • Arterial Hypertension

Sponsors & Collaborators

  • UMC Utrecht

    collaborator OTHER
  • Echosens

    collaborator INDUSTRY
  • MIMETAS BV

    collaborator UNKNOWN
  • Nordic Bioscience A/S

    collaborator INDUSTRY
  • Elevate BV

    collaborator UNKNOWN
  • Leiden University

    collaborator OTHER
  • Amsterdam University Medical Center

    collaborator OTHER
  • Andaluz Health Service

    collaborator OTHER_GOV
  • National Research Council, Institute of Clinical Physiology, Italy

    collaborator OTHER
  • Leiden University Medical Center

    collaborator OTHER
  • Université Libre de Bruxelles

    collaborator OTHER
  • University Hospital, Antwerp

    collaborator OTHER
  • Catholic University of the Sacred Heart

    collaborator OTHER
  • Medical Education Research And Innovation Center S.R.L.

    collaborator UNKNOWN
  • EUROPEAN LIVER PATIENTS ASSOCIATION

    collaborator UNKNOWN
  • Harokopio University

    collaborator OTHER
  • General University Hospital, Prague

    collaborator OTHER
  • Novo Nordisk A/S

    collaborator INDUSTRY
  • Maastricht University

    collaborator OTHER
  • Mercodia Aktiebolag

    collaborator UNKNOWN
  • EXIT071 BV

    collaborator UNKNOWN
  • European Atherosclerosis Society

    collaborator OTHER
  • MetaDeq Limited

    collaborator UNKNOWN
  • Associação para Investigação e Desenvolvimento da Faculdade de Medicina

    collaborator UNKNOWN
  • Institute of Cardiometabolism and Nutrition, France

    collaborator OTHER
  • University Hospital, Saarland

    collaborator OTHER
  • Roche Pharma AG

    collaborator INDUSTRY
  • Inventiva Pharma

    collaborator INDUSTRY
  • Biocellvia

    collaborator UNKNOWN
  • Franciscus Gasthuis & Vlietland (Hospital)

    collaborator OTHER
  • Julius Clinical

    lead INDUSTRY

Principal Investigators

  • Manuel Castro Cabezas, MD/PhD · Sint Franciscus Gasthuis

  • Diederick E. Grobbee, MD/PhD/FESC · UMC Utrecht

  • Oscar H. Franco, MD/PhD/FESC/FFPH · UMC Utrecht

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-30
Primary Completion
2031-03-31
Completion
2031-03-31

Countries

  • Belgium
  • Czechia
  • France
  • Germany
  • Greece
  • Italy
  • Netherlands
  • Portugal
  • Romania
  • Spain

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05651724 on ClinicalTrials.gov