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Screening for metabolically related fatty liver disease and cirrhosis in people with type 2 diabetes

Screening for metabolically related fatty liver disease and cirrhosis in people with type 2 diabetes

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064859
Enrollment
Unknown
Registered
2022-10-20
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

metabolically related fatty liver disease

Interventions

Group of type 2 diabetes mellitus with metabolism-related fatty liver disease:None

Sponsors

Zhongda Hospital Affiliated to Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. According to the Chinese Guidelines for the Prevention and Treatment of Type 2 Diabetes, the patient was diagnosed with T2DM; 3. Liver hardness and fat attenuation parameters were measured based on iLivTouch; 4. The subject (or his legal guardian) understands the requirements of the clinical trial and has signed an informed consent prior to performing any special tests related to the trial; 5. Subjects agree to and are able to complete all follow-up evaluations required for this study.

Exclusion criteria

Exclusion criteria: 1. Confirmed cases of viral hepatitis and hepatic schistosomiasis; 2. A diagnosis of malignancy or high risk of cancer/recurrence, or a life expectancy of less than 60 months; 3. Currently participating in clinical trials of other drugs or medical devices, and have not yet completed the primary study endpoint of the study; 4. Pregnant or lactating patients, or patients who plan to become pregnant within 1 year (women of childbearing age must undergo a pregnancy test within 7 days prior to baseline surgery); 5. History of alcohol/drug/substance abuse; 6. Conditions that affect subject safety or otherwise interfere with the evaluation of test results as determined by the investigator; 7. Patients with incomplete data.

Design outcomes

Primary

MeasureTime frame
incidence;risk factors;

Countries

China

Contacts

Public ContactLi Ling
dr_liling@126.com+86 13951606816

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026