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Exploring Biomarkers Predicting the Outcome of Acute-on-chronic Liver Failure

A Study on Biomarkers Predicting the Outcome of Acute-on-chronic Liver Failure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02965560
Acronym
PGE2
Enrollment
350
Registered
2016-11-16
Start date
2016-10-10
Completion date
2018-06-01
Last updated
2018-06-06

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

Conditions

Acute-On-Chronic Liver Failure, Cirrhosis and Chronic Liver Disease

Brief summary

Acute-on-chronic liver failure (ACLF) is an ailment with high incidence of multiorgan failure (MOF) and consequent mortality. Systemic inflammation and susceptibility to infection are characteristic pathophysiological features. Prostaglandin E2 (PGE2) could subdue systemic inflammation and alleviate liver injury in mice model. However, there are no studies evaluating PGE2 as a predictor of early mortality.This study is designed to investigate whether plasma PGE2 and its receptors are associated with development of MOF and predict short-term mortality in patients with acute-on-chronic liver failure. By the way, we will also measure several other potential predictive factors (C-reactive protein,severe hyponatremia, Second infections,Diabetes mellitus,High density lipoprotein,interleukin-10,serum bile acids,ferritin,the neutrophil to lymphocyte ratio,soluable urokinase plasminogen activator receptor,vWF-Ag levels and FVIII-to-PC ratios).

Interventions

DIAGNOSTIC_TESTplasma suPAR, PGE2 measurement. Other biomarkers were just recorded from clinical laboratory.

Sponsors

First Affiliated Hospital of Zhejiang University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Clinical diagnosis of acute-on-chronic liver failure according to Asian-Pacific Association for the Study of the Liver (APASL) diagnostic criteria

Exclusion criteria

* Hepatocellular carcinoma(HCC) * Portal vein thrombosis * Pregnancy * Human immunodeficiency virus (HIV) * Patients who had received immunomodulator,or cytotoxic/immunosuppressive therapy within at least the preceding 12 months

Design outcomes

Primary

MeasureTime frame
all cause mortality90 days
incidence of multiorgan failure90 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026