Assessment of a hepatomiR Cut-off for Predicting Specific Hepatic Decompensation Events in Advanced Chronic Liver Disease

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

This study looks to gather data on hepatomiR, a CE-certified test already intended for gauging liver-related outcomes, in order to define a cut-off regarding specific decompensation events (ascites, variceal hemorrhage, hepatic encephalopathy) in chronic liver disease (CLD). Based on these data, it is aimed to advance the current understanding of factors driving decompensation, with potential repercussions for future risk management and therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years

• Chronic liver disease (more than 6 months)

• LSM ≥ 10 kPa

• Outpatient at the Clinical Department of Internal Medicine II, University Hospital St. Pölten

• Signed patient consent form

Locations
Other Locations
Austria
University Hospital St. Pölten
RECRUITING
Sankt Pölten
Contact Information
Primary
Lukas Erhart, Mag. Dr.
lukas.erhart@stpoelten.lknoe.at
00432742900412311
Time Frame
Start Date: 2024-05-15
Estimated Completion Date: 2026-06
Participants
Target number of participants: 156
Treatments
cACLD
Patients with compensated advanced chronic liver disease (cACLD) regardless of etiology
Sponsors
Collaborators: University Hospital St. Polten
Leads: Karl Landsteiner University of Health Sciences

This content was sourced from clinicaltrials.gov