Clinical Trial

Korean Real-world Study on MASLD/MASH Outcomes.

Active, Not Recruiting
View on ClinicalTrials.gov →
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.
Trial Details
NCT Number NCT07739901
Lead Sponsor Novo Nordisk A/S
Conditions MASLD/MASH
Enrollment 10,000 participants
Start Date 2026-07-13
Primary Completion 2026-09-30 (estimated)
Study Completion 2026-09-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-31