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ACTIVE NOT RECRUITING
NCT07739901

Korean Real-world Study on MASLD/MASH Outcomes.

Sponsor: Novo Nordisk A/S

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.

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

OTHER

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