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A study and analysis of serum inflammatory factor levels in patients with liver cirrhosis

A study and analysis of serum inflammatory factor levels in patients with liver cirrhosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110095
Enrollment
Unknown
Registered
2025-09-30
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Cirrhosis

Interventions

Healthy control group:None

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 75 Years

Inclusion criteria

Inclusion criteria: Subject Inclusion Criteria:All selected candidates were diagnosed based on the Guidelines for the Diagnosis and Treatment of Liver Cirrhosis and the Guidelines for the Prevention and Treatment of Chronic Hepatitis B (2019 Edition) published by the Hepatology Branch of the Chinese Medical Association. The diagnosis of cirrhosis requires a comprehensive consideration of etiology, medical history, clinical manifestations, complications, treatment process, testing, imaging and histology. All enrolled patients met the diagnostic criteria for liver cirrhosis by clinical, imaging (ultrasound, CT, MRI), or liver biopsy (e.g., Metavir score F4, Ishak score 5-6). Inclusion criteria for the healthy control group: 1. Age between 16 and 75 years old; 2. No cirrhosis and liver fibrosis related pathological states; 3. No serious chronic diseases, such as cardiovascular disease, liver and kidney failure, malignant tumors, etc.; 4. The results of physical examination and basic laboratory tests (liver function, coagulation function, etc.) are within the normal range; 5. No family history of liver cirrhosis and liver fibrosis; 6. No history of hepatitis virus, schistosomiasis and other related exposures.

Exclusion criteria

Exclusion criteria: 1.Exclusion criteria for subjects: (1) Those with missing clinical data were excluded; (2) Exclude patients with cardiovascular disease, diabetes, primary kidney disease, hematological disease, malignant tumor, etc.; (3) Previous liver transplantation; (4) Patients infected with human immunodeficiency virus and new coronavirus; (5) Patients who have used blood products in the past 1 month; (6) Patients with elevated procalcitonin and obvious acute bacterial infection and sepsis; (7) Patients with rheumatic immune system diseases; (8) Patients who died from non-liver disease causes. 2.Exclusion Criteria: (1) Suffering from acute and chronic hepatitis, liver fibrosis and cirrhosis-related diseases;(2) There are comorbidities that may interfere with the results, such as autoimmune diseases, active infection, etc; (3) Recent (within 3 months) use of drugs that may affect the research results, such as immunosuppressants, hormones, etc; (4) Participate in other clinical trials or receive special treatment, such as surgery, radiotherapy, etc; (5) Pregnant or lactating women; (6) Long-term alcoholism, drug abuse, etc.

Design outcomes

Secondary

MeasureTime frame
Levels of inflammatory markers;

Countries

China

Contacts

Public ContactHong Rutao

The First Affiliated Hospital of Anhui Medical University

hongrutaoah@aliyun.com+86 551 65908683

Outcome results

None listed

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