Clinical Trials Directory

Trials / Completed

CompletedNCT04677101

Liquid Biopsy for NASH and Liver Fibrosis

Liquid Biopsy as a Non-invasive Tool for the Diagnosis of NASH and Liver Fibrosis

Status
Completed
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Catholic University of the Sacred Heart · Academic / Other
Sex
All
Age
Healthy volunteers

Summary

Nonalcoholic fatty liver disease (NAFLD) has evolved to represent the most common cause of chronic liver disease globally. Today, NAFLD is a leading indication for liver transplantation and a major etiology for hepatocellular carcinoma (HCC) in the United States. NAFLD is characterized by the excess accumulation of lipids within the liver and ranges from isolated steatosis to nonalcoholic steatohepatitis (NASH), which is characterized by the presence of hepatic necroinflammation, hepatocyte ballooning and fibrosis progression. Currently, liver biopsy remains the gold standard for the diagnosis of various chronic liver diseases, and for determining the severity of liver injury, inflammation, and fibrosis stage. However, this procedure is invasive, prone to complications such as bleeding and is associated with sampling variability and limited representation of the whole liver. Other limitations include, the difficulty to monitor liver injury progression over time and underestimation of disease severity. Despite intensive research, currently available non-invasive blood tests are not sufficiently sensitive or specific and are therefore of limited use. Blood biomarkers might provide significant advances in the diagnosis and monitoring of disease progression and regression in clinical settings. Recently, liquid biopsy has emerged as a potential, less invasive, alternative to liver biopsy. In fact, it addresses several unmet clinical needs, including sensitivity, specificity, the determination of prognoses, and the prediction of therapeutic responses.

Detailed description

This is a multicentric prospective observational study to validate blood non-invasive biomarkers for NASH and fibrosis stage. 150 subjects will be enrolled; 100 subjects with biopsy-proven NASH and 50 subjects with normal liver will be used as controls.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTLiver BiopsyFine-needle liver biopsy

Timeline

Start date
2020-12-16
Primary completion
2021-03-16
Completion
2021-04-16
First posted
2020-12-21
Last updated
2021-05-19

Locations

2 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT04677101. Inclusion in this directory is not an endorsement.