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Construction of a fatty liver disease cohort in populations with metabolic risk factors and clinical translational research

Construction of a fatty liver disease cohort in populations with metabolic risk factors and clinical translational research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121334
Enrollment
Unknown
Registered
2026-03-30
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

metabolic dysfunction-associated steatotic liver disease

Interventions

Observation group:none

Sponsors

The First Affiliated Hospital, College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age = 18 years and < 80 years; 2. Have metabolic risk factors (obesity, type 2 diabetes, dyslipidemia, hypertension, etc.); 3.Have undergone FibroScan non-invasive assessment, which can provide liver stiffness (LSM) and liver fat content (CAP value) for baseline and follow-up analysis.

Exclusion criteria

Exclusion criteria: 1. Patients with other clear liver diseases during the baseline or follow-up period, including those with positive hepatitis B surface antigen, those with active hepatitis C infection that has not been cured, drug-induced liver injury, autoimmune liver disease, and hereditary liver disease, etc. 2.Patients with active viral infections, such as HIV infection or other active infections that may affect liver function and metabolism, to avoid confounding factors interfering with the analysis. 3.Patients with malignant tumors at baseline or within the previous five years are excluded to prevent the interference of tumors and related treatments on liver and metabolic status. 4. Pregnant or lactating women are excluded to avoid the influence of physiological conditions on liver lipid metabolism and fluid status. 5.Patients who have not completed key examinations or have missing key follow-up data are excluded, such as those lacking FibroScan, imaging or laboratory indicators, to ensure the completeness of the main evaluation indicators.

Design outcomes

Primary

MeasureTime frame
The prevalence rate of MASLD;

Secondary

MeasureTime frame
Liver fibrosis and fat content;Liver-related events;metabolism-related complications;

Countries

China

Contacts

Public ContactYu Shi

The first affiliated hospital, Zhejiang University School of Medicine

zjushiyu@zju.edu.cn+86 135 8812 2303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026