ClinicalTrials.Veeva

Menu

A Real-world Assessment in Implementation of the MASH Patient Care Pathway in Chinese Population Using the Meinian Health Check-up Database (IMPACT MASH)

Novo Nordisk logo

Novo Nordisk

Status

Completed

Conditions

Metabolic Dysfunction-associated Steatotic Liver Disease (MASLD) & Steatohepatitis (MASH)

Treatments

Other: No treatment given

Study type

Observational

Funder types

Industry

Identifiers

NCT06741111
U1111-1308-1064 (Other Identifier)
DAS-8256

Details and patient eligibility

About

The primary objective of this study is to estimate the proportion of people with low/intermediate/high risk of advanced fibrosis in at risk Chinese population based on the European Association for the Study of the Liver (EASL) 2024 care pathway

Enrollment

1,233,970 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

For All and Study population:

  1. Male or female, age above or equal to 18 years on health-check-up visit day
  2. No missing value on sex

For EASL at risk population

  1. Must be part of study population.
  2. People with T2D or [obesity+above or equal to 1 cardiometabolic risk factor(s)] or elevated liver enzymes

For EASL not at-risk population

  1. Must be part of study population.

For EASL-SAFE

  1. Must be part of EASL at risk population

For AGA at risk population

  1. Must be part of study population.
  2. People with 2 or more metabolic risk factors (EASL-MASLD criteria) or T2D or steatosis on any imaging modality or with elevated aminotransferases

For CSH MAFLD population

  1. Must be part of study population.
  2. Liver steatosis on abdominal ultrasound
  3. With at least one component of Metabolic syndrome (MetS [CSH])

Exclusion criteria

  1. Individuals originating from centers with fewer than 100 participants
  2. Missing value of liver stiffness measurement (LSM)
  3. Had an interquartile range/median ratio above or equal to 30% of the measurement of LSM
  4. Missing value on either aspartate aminotransferase (AST) or alanine aminotransferase (ALT) or platelet count (PLT)
  5. Missing value on FPG, TG, HDLc or BP (to define the presence of metabolic risk factors)
  6. Missing value on abdominal ultrasound

For EASL not at-risk population 1. People with T2D or [obesity+above or equal to 1 cardiometabolic risk factor(s)] or elevated liver enzymes

For EASL-SAFE/NFS

  1. Missing value on globulin

Trial design

1,233,970 participants in 1 patient group

Cohort
Description:
People who underwent health check-up in Meinian check-up centres between the period January 1st, 2023, to December 31st, 2023
Treatment:
Other: No treatment given

Trial contacts and locations

1

Loading...

Central trial contact

Novo Nordisk

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems