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Non-Invasive Evaluation of Fibrosis and Steatosis in Chronic Hepatopathy

T

Tischendorf, Jens, M.D.

Status

Unknown

Conditions

Steatohepatitis
Chronic Liver Disease
Fibrosis

Study type

Observational

Identifiers

NCT01246388
LU-TI-01

Details and patient eligibility

About

The purpose of this study is to evaluate non-invasive parameters for staging and grading of chronic hepatopathy in comparison to liver biopsy.

Full description

For diagnosis, staging and grading of chronic liver disease, liver biopsy is the gold standard to date. Unfortunately, being an invasive diagnostic method, liver biopsy has a significant morbidity. Furthermore, due to the small sample size, sampling error (over- or underestimating severity of liver disease) is a serious problem in diagnostic of chronic liver disease.

The objective of this study is to evaluate non-invasive diagnostic methods (MRI, elastography, ultrasound and serum parameters) in comparison to the gold standard to establish criteria for diagnostic in liver disease and reduce the necessary amount of liver biopsies in the future and allow regular follow up.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic hepatopathy and necessity of liver biopsy

Exclusion criteria

  • metal implants preventing MRI

Trial design

50 participants in 1 patient group

Chronic Liver Disease

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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