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Body Composition and Fatty Liver Disease

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Seoul National University

Status

Active, not recruiting

Conditions

Fatty Liver

Treatments

Diagnostic Test: Non-contrast low-dose abdomen CT
Diagnostic Test: bioelectrical impedance analysis (BIA)
Diagnostic Test: Fibroscan

Study type

Interventional

Funder types

Other

Identifiers

NCT05695118
SNUH-2022-3238

Details and patient eligibility

About

This study investigates relationship between fatty liver prognosis and body composition analysis result based on non-contrast low dose CT in patients with fatty liver disease.

Enrollment

150 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • metabolic dysfunction-associated fatty liver disease (fatty liver with overweight/obesity, or type II DM or other metabolic dysfunction)
  • or non-alcoholic fatty liver disease with liver function test abnormality
  • signed informed consent

Exclusion criteria

  • chronic hepatitis B or C
  • other disease related to fatty liver such as glycogen storage disease, lipodystrophy, familial combined hyperlipidemia, hypobetalipoproteinemia, Weber-Christian syndrome or abetalipoproteinemia
  • on medication related to hepatic steatosis (tamoxifen, steroid, valproic acid, methotrexate, amiodarone)
  • diabetes after pancreatectomy
  • history of total parenteral nutrition in 6 months
  • pregnancy or nursing mother

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

150 participants in 1 patient group

non-contrast low-dose abdomen CT
Experimental group
Description:
non-contrast low-dose abdomen CT (target effective dose: \< 1.5 mSv). CT based body composition analysis is performedd with commercially available automatic segmentation software (DeepCatch, Medical IP, South Korea).
Treatment:
Diagnostic Test: Fibroscan
Diagnostic Test: bioelectrical impedance analysis (BIA)
Diagnostic Test: Non-contrast low-dose abdomen CT

Trial contacts and locations

1

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Central trial contact

Jeong Hee Yoon, MD; Hyuna Jung

Data sourced from clinicaltrials.gov

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