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Plasma MicroRNA for Prediction of Hepatocellular Carcinoma

B

Benha University

Status

Completed

Conditions

Hepatitis C

Treatments

Biological: Blood Sampling

Study type

Observational

Funder types

Other

Identifiers

NCT05449847
RC 1.7.2021

Details and patient eligibility

About

100 patients with diagnosed HCV were evaluated by clinical and ultrasound examination and were categorized as uncomplicated HCV (n=22) and complicated HCV (n=78). All patients were evaluated for hepatosteatosis and liver fibrosis using the computerized hepatorenal index, the hepatic steatosis index, aspartate aminotransferase (AST)/platelet count index (APRI) and the Fibrosis-4 (FIB-4) scores. Blood samples were obtained for estimation of serum levels of liver function tests and plasma levels of microRNA 21 and 126.

Enrollment

100 patients

Sex

All

Ages

31 to 67 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Complicated hepatitis C by HCC
  • Complicated hepatitis C by liver cirrhosis
  • Complicated hepatitis C by steatohepatitis
  • uncomplicated hepatitis C

Exclusion criteria

  • pre-portal fibrosis secondary to previous bilharzial disease
  • pre-portal fibrosis secondary to alcoholic fatty liver
  • The presence of hepatic malignancy other than HCC
  • decompensated cirrhosis
  • hepatorenal failure
  • hepatic manifestations of congestive heart failure.

Trial design

100 participants in 2 patient groups

Complicated HCV
Treatment:
Biological: Blood Sampling
Non Complicated HCV
Treatment:
Biological: Blood Sampling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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