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Clinical study of metabonomics combined with proteomic detection to explore blood markers in the process of liver inflammation and cancer transformation

Clinical study of metabonomics combined with proteomic detection to explore blood markers in the process of liver inflammation and cancer transformation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102288
Enrollment
Unknown
Registered
2025-05-13
Start date
2024-08-04
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Hepatitis and cancer transformation

Interventions

Liver Disease:None
Control:None
Hepatic fibrosis:None
compensatory Liver cirrhosis:None
Liver Cancer:None

Sponsors

The Second Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.(1) patients with hepatitis B and patients with non-alcoholic fatty liver disease in the liver disease group met the diagnostic criteria of the guidelines for Prevention and treatment of chronic Hepatitis B (2022 Edition). Inclusion criteria for patients with non-alcoholic fatty liver disease: in accordance with the diagnostic criteria of the guidelines for the Prevention and treatment of non-alcoholic Fatty liver Disease (updated 2018); According to Metavir staging and liver transient elastic ultrasound, the patients were divided into two groups: non-fibrosis group and fibrosis group (including significant fibrosis and progressive fibrosis): 1). normal ALT with LSM 2; PLT 1.3 Albumin 2cm;3) at the same time, the tumor marker alpha-fetoprotein (AFP) >= 400ug / kg, excluding pregnancy, hepatitis or metastatic liver cancer; 4) liver histopathological examination conformed to the diagnostic criteria of primary hepatocellular carcinoma (HCC); 5) according to the CSCO2023 guidelines for primary liver cancer, TNM stage belonged to early and middle stage (I, II, III); 6) there were complete data of anti-tumor treatment. 2.Control group: select healthy individuals who underwent physical examinations at the hospital during the same period, with normal liver function indicators.

Exclusion criteria

Exclusion criteria: 1.(1) patients who do not meet the above inclusion criteria; (2) hepatitis, cirrhosis and liver cancer caused by other liver diseases, such as autoimmune liver disease, drug-induced liver damage, alcoholic liver disease, etc.; (3) complicated with severe heart, kidney and hematopoietic system diseases, patients with other tumor diseases, mental illness; (4) pregnant or lactating women. 2.Control group: history of hepatitis, liver function damage, major surgeries, and diseases.

Design outcomes

Primary

MeasureTime frame
Metabonomics;Proteomics;

Secondary

MeasureTime frame
Total cholesterol;Triglycerides;Low-density lipoprotein cholesterol;High-density lipoprotein cholesterol;TCM syndrome scale;

Countries

China

Contacts

Public ContactSun Tao

The Second Affiliated Hospital of Zhejiang Chinese Medical University (Xinhua Hospital of Zhejiang Province)

326516058@qq.com+86 182 5829 6259

Outcome results

None listed

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