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Establishment of a Prognostic Model for Hepatitis B-Related Acute-on-Chronic Liver Failure

Establishment of a Prognostic Model for Hepatitis B-Related Acute-on-Chronic Liver Failure Based on Non-Coding RNA in Serum Extracellular Vesicles Before and After Artificial Liver Treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115091
Enrollment
Unknown
Registered
2025-12-22
Start date
2025-12-26
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Hepatitis B associated chronic acute liver failure (HBV-ACLF)

Interventions

Group A acute progressive type:N/A
Group B acute recovery type:N/A
Group C slow progressing type:N/A
D group slow recovery type:N/A
Group E slow and persistent type:N/A
The control group compensated hepatitis B cirrhosis:N/A

Sponsors

Tianjin Third Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18-75 with HBV-ACLF, whose ACLF diagnostic criteria comply with the "Diagnosis and Treatment Guidelines for Liver Failure (2024 Edition)" Diagnostic criteria for acute liver failure. 2.Receives antiviral treatment and artificial liver treatment (2-3 times a week) as well as internal medicine support. 3.Patients with HBV-ACLF who received treatment and were followed up for 90 days with complete data.

Exclusion criteria

Exclusion criteria: 1. Concurrent alcoholic hepatitis, autoimmune hepatitis, genetic metabolic hepatitis 2. Diagnosed or suspected concurrent liver cancer or other malignant tumors; 3.There are serious basic diseases of extrahepatic organs: severe chronic obstructive pulmonary disease with respiratory failure, severe coronary heart disease with heart failure, severe complications of diabetes, chronic kidney disease with renal failure; 4.Clinical information and laboratory examination data are missing or incomplete;Unable to cooperate or refuse to accept follow-up.

Design outcomes

Primary

MeasureTime frame
RNA differentially expressed: miRNAs, lncRNAs, and circRNAs;

Countries

China

Contacts

Public ContactLiang Jing

Tianjin Third Central Hospital

haolele77@sina.com+86 22 8411 2310

Outcome results

None listed

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