ClinicalTrials.Veeva

Menu

Early Detection of Advanced Fatty Liver Disease

H

HaEmek Medical Center, Israel

Status

Completed

Conditions

Liver Fibrosis
Non-alcoholic Fatty Liver Disease

Study type

Observational

Funder types

Other

Identifiers

NCT03608748
007-18-EMC

Details and patient eligibility

About

Non-alcoholic fatty liver disease is the most common cause of chronic liver disease in the western world, affecting one in every three subjects.

The investigators hypothesize that a patient population without known liver disease has a certain percentage of patients with liver fibrosis who are undiagnosed and not monitored.

Full description

The investigators will run an algorithm for the non-invasive diagnosis of advanced fibrosis in non-alcoholic fatty liver disease on a participants without known liver disease.

Nafld Score and Elastography are now being used to predict the severity of liver fibrosis and deciding whether the patient is going to a biopsy, clinical follow-up or further investigation of liver cirrhosis and complications.

The detection of participants with Nafld Score more than 0.675 (advanced fibrosis) will enroll them to an elastography test. Participants with advanced fibrosis according to elastography will be introduced to follow-up and treatment that should delay or prevent progression of the disease to more advanced conditions like: cirrhosis, portal hypertension, esophageal varicose veins and hepatocellular carcinoma.

If the investigators find that the results of the study are consistent with their hypothesis, this will lead to applying the flowchart to a larger sample of population in order to use it as a future survey.

Moreover, the investigators will check whether there is a correlation between Nafld Score and elastography in participants without know liver disease with Nafld Score more than 0.675.

Enrollment

1,000 patients

Sex

All

Ages

45 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Subjects aged 45-60 who belong to an initial clinic which was chosen arbitrarily.
  2. Subjects without known liver disease.
  3. Subjects agree to sign a consent form. -

Exclusion criteria

  1. History of right-sided heart failure
  2. History of liver disease including positive infectious serology for hepatitis B or C
  3. Pregnant women
  4. People incapable of judgment -

Trial contacts and locations

1

Loading...

Central trial contact

Habib Abu Shqara, Dr; Rawi Hazzan, Dr

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems