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Clinical Trials/NCT05720663
NCT05720663RecruitingNot Applicable

Predicting Outcomes in Nonalcoholic Steatohepatitis With Advanced Fibrosis

Virginia Commonwealth University2 sites in 1 country240 target enrollmentStarted: April 19, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
240
Locations
2
Primary Endpoint
Hepatic Encephalopathy (HE)

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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)

Outcomes

Primary Outcomes

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.

Number of deaths

Time Frame: Up to 2 years

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

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.

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.

Secondary Outcomes

  • Model For End-Stage Liver Disease (MELD) score(Up to 2 years)
  • Hepatocellular cancer (HCC)(Up to 2 years)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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