Multi-parametric Magnetic Resonance Imaging for the Precise Diagnosis and Quantitative Study of Liver Steatosis, Inflammation, and Fibrosis in Chronic Liver Disease.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorShengjing Hospital

About this trial

To construct a novel, non-invasive, accurate, and convenient method to achieve the degree of liver damage is an important general problem in the management of patients with chronic liver disease. The investigators would like to develop non invasive advanced Magnetic Resonance Imaging (MRI) techniques (MR elastography, MRI-PDFF) to assess the degree of liver damage in patients with chronic liver disease. These techniques could reach high diagnostic performance for detection of liver fibrosis, inflammation and liver fat content; and could decrease the number of liver biopsies, which have risks and sample only a small portion of the liver.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Chronic liver disease (including viral hepatitis, alcoholic hepatitis, non alcoholic steatohepatitis, primary biliary cirrhosis, primary sclerosing cholangitis, etc..)

Age range of 18 to 75 years old

Accept systematic antiviral therapy or hormone or ursodesoxycholic acid or supportive liver protection therapy

Disqualifiers

Age less than 18 years

Unable or unwilling to give informed consent

Contra-indications to MRI

Electrical implants such as cardiac pacemakers or perfusion pumps

Trial population

Treatment-naive patients had already been diagnosed with chronic hepatic disease before enrollment.Patients with liver disease were enrolled in this study to assess the changes in 3D-MRE and MRI-PDFF parameters before and after antiviral therapy or hormone or ursodesoxycholic acid or supportive liver protection therapy.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • 3D-MRE,MRI-PDFF

    Device

    3D-MRE(storage modulus, ., loss modulus and damping ratio \[DR\] for liver inflammation and fibrosis) MRI-PDFF(liver fat content)

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

the changes of liver stiffness assessed by 3D-MRE before and after treatment.

Liver stiffness regression is defined as the change of 3D MRE shear stiffness larger than 19%

Time frame
12 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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