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Prognostic Analysis of Decompensated Liver Cirrhosis Defined by New Pattern of Occurrence and the Discovery and Application of Predictive Markers

Prognostic Analysis of Decompensated Liver Cirrhosis Defined by New Pattern of Occurrence and the Discovery and Application of Predictive Markers+Parallel Project of Excellence 14

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097719
Enrollment
Unknown
Registered
2025-02-25
Start date
2025-02-25
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

liver cirrhosis

Interventions

Acute decompensation group:None
Progressive decompensation group:None
Subclinical decompensation group:None

Sponsors

Beijing Ditan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old; 2. Patients diagnosed with decompensated cirrhosis according to the Guidelines for the Diagnosis and Treatment of Liver Cirrhosis issued by the Hepatology Section of the Chinese Medical Association in 2019; 3. Prospective enrollment and follow-up patients voluntarily participated and signed an informed consent form.

Exclusion criteria

Exclusion criteria: Patients were excluded if they met any of the following exclusion criteria 1. Patients with diagnosis of primary hepatocellular carcinoma; 2. Previous history of nephrotic syndrome, or serum creatinine (Cr) >2 × ULN, or Cr elevation >50 µmol/L or more during the screening period; urinary protein 2+ and above; 3. Combination of other serious diseases, including but not limited to malignant tumor, non-cirrhotic portal hypertension ascites, ischemic heart disease, stroke, chronic obstructive pulmonary disease, and class III-IV heart failure; 4. Organ transplant recipients; 5. Poor patient compliance and inability to complete the visit requirements; 6. Patients whom the investigator considers unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Cumulative mortality associated with liver disease in patients with different patterns of decompensated cirrhosis.;

Secondary

MeasureTime frame
Incidence of cirrhosis-related complications, liver failure, liver transplantation and primary liver cancer in patients with different patterns of decompensated cirrhosis;Risk factors for liver disease-related mortality in patients with decompensated cirrhosis; Predictive value of a risk prediction model for decompensated cirrhosis;Incidence of recompensation in decompensated cirrhosis;

Countries

China

Contacts

Public ContactQi Wang

Center of Liver Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China

wangqidl04@ccmu.edu.cn+86 156 1126 5361

Outcome results

None listed

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