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Korean Real-world Study on MASLD/MASH Outcomes.
Sponsor: Novo Nordisk A/S
Summary
This retrospective multicentre cohort study will use existing medical records from adults with Metabolic Dysfunction-Associated Steatotic Liver Disease or Metabolic Dysfunction-Associated Steatohepatitis (MASLD/MASH) who underwent two Vibration-Controlled Transient Elastography-Liver Stiffness Measurement (VCTE-LSM) (FibroScan) assessments during routine clinical care. The study will evaluate whether changes in fibrosis risk tier between the two assessments are associated with future major liver-related outcomes and all-cause mortality. The duration of study will be 5 months.
Official title: Linking Surrogate Endpoints to Long-term Final Outcomes in MASLD/MASH: A Korean Multicentre Real-World Evidence Study
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
10000
Start Date
2026-07-13
Completion Date
2026-09-30
Last Updated
2026-07-31
Healthy Volunteers
No
Conditions
Interventions
No treatment is given
This is a retrospective observational cohort study. The data will be collected via EMR.
Locations (1)
Novo Nordisk Investigational Site
Seoul, South Korea