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Registry Study for Optimal Management of Liver Failure in the Chinese Population

Registry Study for Optimal Management of Liver Failure in the Chinese Population (RESOLVE-C)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05740696
Acronym
RESOLVE-C
Enrollment
500
Registered
2023-02-23
Start date
2023-01-06
Completion date
2028-12-30
Last updated
2023-02-23

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

Conditions

Liver Failure

Brief summary

Liver failure is the most severe form of liver damage caused by viral, alcoholic, drug-related and ischemia-reperfusion factors, often combined with extrahepatic organ damage, resulting in a high mortality rate. This study intends to construct a real-world case registry database of inpatients with liver failure based on an electronic clinical data collection system through a multicenter collaborative network to study the clinical characteristics, epidemiology of bacterial and fungal infections, the impact of sarcopenia on clinical prognosis, and optimization of treatment strategies such as antiviral and artificial liver in Chinese inpatients with liver failure. The cohort and experience generated from this study will be used as a support for a series of future studies to focus on clinical issues such as infection, end-stage liver disease combined with organ failure, and early warning of critically ill patients.

Interventions

PROCEDUREALF

Acute onset, no history of underlying liver disease, liver failure characterized by degree Ⅱ or above hepatic encephalopathy developed within 2 weeks

PROCEDURESALF

The onset was acute, with no history of underlying liver disease, and clinical manifestations of liver failure appeared between 2 and 26 weeks

PROCEDUREACLF

On the basis of chronic liver disease, the clinical manifestations of acute liver decompensation and liver failure appear in a short period

Sponsors

First Affiliated Hospital Xi'an Jiaotong University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Patients with a diagnosis consistent with liver failure and pre-liver failure: * Extreme weakness with significant gastrointestinal symptoms such as anorexia, vomiting and abdominal distention; * Elevated alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) with progressive jaundice (TBil≥85.5 μmol/L); * Bleeding tendency with PTA ≤ 60% or INR ≥ 1.5.

Exclusion criteria

* An event or complication that, in the judgment of the investigator, significantly affects the assessment of clinical status.

Design outcomes

Primary

MeasureTime frameDescription
Overall survival28-day28-day survival rates without liver transplantation

Secondary

MeasureTime frameDescription
Disease progression48 weeks after dischargeIncidence of complications and re-hospitalization at 48 weeks after discharge

Countries

China

Contacts

Primary ContactYingli He, Pro.
heyingli2000@xjtu.edu.cn0086-18991232863
Backup ContactJuan Li, M.D.
lijuan1996xx@163.com0086-18209272726

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026