Fatty Liver Disease in Nordic Countries

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCopenhagen University Hospital, Hvidovre

About this trial

A prospective cohort study, which aims to systematically evaluate biomarkers and potential targets in NAFLD and NASH.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Non-alcoholic fatty liver disease and

Healthy volunteers

Disqualifiers

Other liver diseases than non-alcoholic fatty liver disease

Lack of informed consent

Trial population

The investigators plan to include patients with suspected or verified non-alcoholic fatty liver disease

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Proteomics

    Diagnostic test

    Mass-spectometry proteomics

  • Transcriptomics

    Diagnostic test

    Next generation sequencing

  • Genomics

    Genetic

    Targeted genetics

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Fibrosis

Number of participants with fibrosis proression

Time frame
5 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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