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NCT Number: NCT05720663

Predicting Outcomes in Nonalcoholic Steatohepatitis With Advanced Fibrosis

Nonalcoholic Steatohepatitis (NASH) is a condition with increased amount of fat, inflammation and scarring in the liver. In compensated cirrhosis, the liver is coping with this damage and maintaining its important functions. Decompensation occurs when the liver becomes unable to perform all of its functions adequately. Variceal hemorrhage (bleeding from abnormal vessels in the liver called varices), Ascites (abnormal build-up of fluid in the abdomen), and Encephalopathy (brain confusion as a result of the liver not being able to get rid of toxic substances) are three symptoms of liver decompensation.

The purpose of this research study is to investigate better ways to routinely monitor the condition of patients with NASH with compensated cirrhosis and to better pinpoint the development of decompensation in the livers of these patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Mayo Clinic in Rochester, Rochester, Minnesota, United States

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About this study

This clinical research study is done to investigate better ways to routinely monitor the condition of patients with Nonalcoholic Steatohepatitis (NASH) with compensated cirrhosis. The purpose of this study is to better pinpoint the development of decompensation in the livers of these patients (some symptoms are variceal hemorrhage, ascites, and encephalopathy, defined below).

NASH is a condition with increased amount of fat, inflammation and scarring in the liver. In compensated cirrhosis, the liver is coping with this damage and maintaining its important functions. Decompensation occurs when the liver becomes unable to perform all of its functions adequately. Variceal hemorrhage (bleeding from abnormal vessels in the liver called varices), Ascites (abnormal build-up of fluid in the abdomen), and Encephalopathy (brain confusion as a result of the liver not being able to get rid of toxic substances) are three symptoms of liver decompensation.

Aside from current routine procedures including blood draws, this study will check to see how effectively adding three additional procedures will help predict development of liver decompensation. These additional procedures are Spleen Stiffness Measurement (SSM) during a special liver ultrasound called a Fibroscan, an imagining scan called Magnetic Resonance Imagining (MRI) using a contrast agent called Gadoxetate Sodium to highlight cirrhosis, and an MRI scan called metabophenotype, which examines muscle composition of the liver.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Adult patients with presence of NAFLD associated cirrhosis.

  • Cirrhosis: biopsy confirmed or Agile F (F4) score > 0.45
  • NAFLD as an etiology of liver disease will be determined based on presence of any of the following:
  • Biopsy showing >5% steatosis or
  • CAP > 280 dB/m or MR-PDFF>5%
  • If CAP < 280 dB/m or MR-PDFF <5%, then must have type 2 diabetes and or 2 or more features of metabolic syndrome for 5 years (cryptogenic cirrhosis)

Exclusion criteria

  • Refusal to consent
  • Alcohol use > 14/21 gm/week cutoff
  • Other causes of chronic liver disease
  • MELD > 12
  • Hepatic and extrahepatic cancers expected to limit life expectancy < 2 yrs
  • prior hepatic resections, TIPS, splenic embolization
  • prior decompensation events
  • inability to fit into MRI (failed hula-hoop test)
  • general contraindication for MRI contrast (GFR < 30 ml/min)
  • contraindications for MRI
  • pregnancy
  • acute kidney injury
  • reduced kidney function (GFR <30ml/min)

Treatment and study plan

Standard of care

Other

Participants will receive the standard of care for their condition

Primary outcomes

  1. Number of deaths

    Time frame: Up to 2 years

    Number of deaths will be determined from death records and patient charts.

  2. Incidents of variceal hemorrhage

    Time frame: Up to 2 years

    Number of participants showing bleeding from abnormal vessels in the liver called varices will be assessed using an endoscopy exam.

  3. Incidents of ascites

    Time frame: Up to 2 years

    Number of participants with experiencing abnormal build-up of fluid in the abdomen will be assessed using a clinical exam including an ultrasound graded per clinical standards.

  4. Hepatic Encephalopathy (HE)

    Time frame: Up to 2 years

    Number of grade 2, 3, or 4 HE events will be assessed by clinician during exams.

Secondary outcomes

  1. Model For End-Stage Liver Disease (MELD) score

    Time frame: Up to 2 years

    Number of participants with MELD scores greater than 15

  2. Hepatocellular cancer (HCC)

    Time frame: Up to 2 years

    Number of participants with HCC

Study contacts

Contact information is provided by the study sponsor or research team.

Mohammad S Siddiqui, MD

CONTACT

[email protected]

804-828-4060

Sponsors and collaborators

Lead sponsor

Virginia Commonwealth University

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Feb 9, 2023
Registry last updated
Apr 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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