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CompletedNCT00770198Updated Oct 9, 2008

sgp130 in Chronic Human Liver Disease

An observational study in Alcoholic Liver Disease and Chronic Hepatitis C Virus Infection, sponsored by Erasme University Hospital. Completed at 1 site in Belgium. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2008-10-09.

Sponsored by Erasme University Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
129
Ages
18 Years and older
Sex
All
01

Study summary

Chronic liver disease are characterized by increased levels of plasma IL-6, but the bioactivity of this cytokine in this disease is not well known. IL-6 receptor complex is regulated by multiple receptors subunits: the soluble form of IL-6 Receptor enhance IL-6 signal by a process called trans-signaling on cells expressing few membrane IL-6 receptors. Soluble gp130 is the natural inhibitor of IL-6 trans-signaling. The aim of this study is to characterize circulating and liver levels of theses compounds of IL-6 receptor complex, to unravel the bioactivity of IL-6 in this disease.

Read the detailed description

Consecutive patients undergoing transjugular liver biopsies for alcoholic liver disease or hepatitis C virus infection will be included in the study to measure plasma cytokines levels, peripheral blood mononuclear cells cytokine release and liver IL-6R compounds mRNA levels.

02

Conditions studied

  • Alcoholic Liver Disease
  • Chronic Hepatitis C Virus Infection

Keywords

  • liver
  • alcohol
  • HCV
03

In context

Hepatitis C

2,321 studies on the registry are indexed under Hepatitis C; 102 are open to participants now.

This study's enrollment of 129 is below the median of 244 across 567 observational studies indexed under Hepatitis C.

Browse Hepatitis C studies →

Lead sponsor

Erasme University Hospital is the lead sponsor of 178 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

patients of Erasme University Hospital

Inclusion criteria

  • Alcohol excess intake and suspected liver disease
  • Alcohol excess intake and clinical liver cirrhosis
  • chronic hepatitis C virus infection and suspected liver disease
  • chronic hepatitis C virus infection and clinical liver cirrhosis

Exclusion criteria

Exclusion Criteria:

  • other (superimposed) liver disease
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
129 participants (actual)
Biospecimen retention
Samples without dna

Groups and cohorts

  • alcoholic liver disease

    alcoholic liver disease patients undergoing a transjugular liver biospy in our institution

  • chronic HCV hepatitis

    chronic HCV hepatitis patients undergoing a transjugular liver biopsy in our institution

06

Study locations

1 site
  • Hopital Erasme - Dpt of Gastroenterology
    Brussels, 1070, Belgium
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 9, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00770198
Lead sponsor
Erasme University Hospital
First posted
Oct 9, 2008
Start date
Jan 2005
Primary completion
Jan 2007
Completion
Oct 2008
Last update
Oct 9, 2008

Study contacts

Arnaud Lemmers, MD
principal investigator · Erasme Hospital, Gastroenterology Dpt

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2008. You cannot join it, but the record below documents what was studied.

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