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NCT07598916Not yet recruiting

Sarcopenia Among Patients With Metabolic Dysfunction-associated Steatotic Liver Disease

Source: ClinicalTrials.gov · Last updated 20 May 2026

Brief summary (registry, in English)

\- Determination of sarcopenia frequency among patients with metabolic dysfunction-associated steatotic liver disease 2- Exploring the association of sarcopenia with disease state (steatosis grade and fibrosis) among patients with metabolic dysfunction-associated steatotic liver disease

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
120 (estimated)
First submitted
14 May 2026
Start date
1 Jun 2026
Primary completion date
30 Jun 2027
Lead sponsor
Assiut University
NCT number
NCT07598916

What you commit to

  • Study type: Observational
  • Planned participants: 120
  • From 1 Jun 2026 to the primary completion date, 30 Jun 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Medication and/or substance use which may lead to hepatic steatosis and/or injury
  • Use of anabolic steroids

Other illness

  • Chronic hepatitis C virus and/or hepatitis B virus infection
  • Autoimmune hepatitis
  • Hepatic and/or extrahepatic neoplastic disorders
  • Eating disorders
  • Comorbidities such as neuromuscular, pulmonary, and renal disorders

Age

  • Age less than 18 years old or more than 65 years old

Other

  • Pregnant patients
  • Any alcohol consumption

Who the study is looking for

  • The study is intended to include adult patients with metabolic dysfunction-associated steatotic liver disease which will be diagnosed based on imaging study plus one of the following criteria \[8\]:
  • BMI ≥ 25 kg/m2 or waist circumference \> 94 cm in men, \> 80 cm in women
  • Fasting serum glucose ≥ 100 mg/dL (≥ 5.6 mmol/L) or 2-hour post-load glucose level ≥ 140 mg/dL (≥ 7.8 mmol/L) or hemoglobin A1C (HbA1C) ≥ 5.7% or on specific drug treatment
  • Blood pressure ≥ 130/85 mmHg or specific drug treatment
  • Plasma triglycerides ≥ 150 mg/dL (≥ 1.70 mmol/L) or specific drug treatment
  • Plasma high-density lipoprotein (HDL)-cholesterol \< 40 mg/dL (\< 1.0 mmol/L) for men and \< 50 mg/dL (\< 1.3 mmol/L) for women or specific drug treatment For significant steatosis grading, hepatic steatosis index (HSI) will be used (BMI, diabetes mellitus, and aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ratio; cut-off score: \>36). \[9\].
    • For significant fibrosis staging, both liver stiffness measurement and several fibrosis scores will be used. Fibrosis scores will include NAFLD fibrosis score (BMI, age, hyperglycemia, AST/ALT ratio, albumin, and platelet count; cut-off score: ≥ 0.675) \[9\].

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.