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Association of Non-alcoholic Fatty Liver Disease and Coronary Artery Disease

J

Johann Wolfgang Goethe University Hospital

Status

Unknown

Conditions

Nonalcoholic Steatohepatitis (NASH)

Treatments

Device: Controlled Attenuation Parameter (CAP), Echosens, Paris, France
Device: Transient Elastography (FibroScan), Echosens, Paris, France

Study type

Interventional

Funder types

Other

Identifiers

NCT01638832
JWGUHMED1-005

Details and patient eligibility

About

This study will evaluate the association of non-alcoholic fatty liver disease and coronary artery disease. All patients presenting for coronary angiogram will receive the following examination:

  • Transient Elastography and Controlled Attenuation Parameter using the FibroScan
  • blood examination including biochemical markers The results of non-invasive liver steatosis and fibrosis measurement are compared with the results of coronary angiogram concerning the presence or absence of coronary artery disease.

Enrollment

572 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female, 18 years and older
  • Written consent
  • Coronary angiogram planned

Exclusion criteria

  • Patients with mental diseases
  • Pregnancy or lactation
  • Ascites

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Mireen Friedrich-Rust, MD

Data sourced from clinicaltrials.gov

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