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RecruitingNCT02206841

Establishment of NAFLD Cohort and Development of Fibrosis Markers

Establishment of Non-alcoholic Fatty Liver Disease Cohort and Development of Markers to Predict Histologic Progression of Liver Fibrosis

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000 (estimated)
Sponsor
Seoul National University Boramae Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is designed for establishment of non-alcoholic fatty liver disease patients cohort to development of markers to predict histologic progression of liver fibrosis.

Detailed description

* Acoustic radiation force impulse elastography and transient elastography * Liver tissue (frozen tissue, paraffin block) * Whole blood, Serum * Fat amount ratio CT (Visceral adipose tissue, Subcutaneous adipose tissue amount) * Body composition analyzer (InBody scale):Total fat/muscle mass and appendicular skeletal muscle mass * Pulmonary function test with post-bronchodilator response and DLCo * EKG, EchoCG, Heart CT (Coronary calcium score), and Pusle wave velocity (AI index, arterial stiffness) * Brain MRI or CT * Upper esophagogastroscopy and colonoscopy * Berlin score questionnaire and Polysomnography

Conditions

Interventions

TypeNameDescription
PROCEDURELiver biopsyPercutaneously liver biopsy will be performed for evaluate steatosis and fibrosis.
DEVICEARFIAcoustic radiation force impulse (ARFI) imaging will be performed for evaluate fibrosis of liver.
DEVICESWESupersonic shear wave elastography (SWE) will be performed for evaluate fibrosis of liver.
DEVICETransient elastographyTransient elastography will be performed for evaluate fibrosis of liver.

Timeline

Start date
2014-01-01
Primary completion
2029-12-31
Completion
2030-12-31
First posted
2014-08-01
Last updated
2025-05-15

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02206841. Inclusion in this directory is not an endorsement.