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Recruiting NCT06867419

Metabolic Features Effects on FAST Score in MASLD Patients

Observational Metabolic Dysfunction-Associated Steatotic Liver Disease

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Transient Elastography.
Who it may be relevant to
Registry conditions: Metabolic Dysfunction-Associated Steatotic Liver Disease. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Metabolic Features Effect on FibroScan-AST (FAST) Score in Egyptian Patients With Metabolic-Associated Steatotic Liver Disease (MASLD)

Overview

The goal of this observational cross-sectional study is to evaluate the effect of metabolic features on Fibroscan-AST (FAST) score stratification in metabolic dysfunction-associated steatotic liver disease (MASLD) patients in Egypt. Researchers will identify the metabolic risk factors in patients with MASLD. evaluate the effect of metabolic features on stratifying MASLD patients by predicting higher FAST score. Participants will be subjected to history taking, clinical examination, laboratory investigations, abdominal ultrasonography, and transient elastography (Fibroscan) to measure liver stiffness (LSM) and controlled attenuation parameter (CAP). The Non-alcoholic fatty liver disease (NAFLD) fibrosis score and FAST score will be calculated.

Interventions

  • Radiation Transient Elastography
    participants will be subjected to anthropometric measurements, laboratory investigations (complete blood count, liver and kidney functions, lipid profile, virology tests, fasting insulin, fasting sugar, 2 hour postprandial sugar, HbA1c, and HOMA-IR), radiological examination (abdominal ultrasound, Fibroscan). the NAFLD fibrosis score, APRI, FIB-4 score, and FAST score will be calculated.

Primary outcome measures

  • impact of metabolic features on FAST score [Time frame: through study completion, an average of 6 months]

Eligibility criteria

Inclusion criteria

  • All patients with MASLD who had steatosis detected by (VCTE-CAP) elastography

Exclusion criteria

  • Patients with a history of significant alcohol consumption more than 30 g/day in men and > 20 g/day in women.
  • Patients with positive hepatitis B or C virus markers.
  • Patients with autoimmune hepatitis.
  • Patients with any other metabolic liver disease.
  • Patients with hepatic focal lesions.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Ecologic or community

Study locations

Egypt · 1 center
  • Tanta University Hospitals — Tanta

Identifiers

NCT: NCT06867419 · 36264PR889/10/24

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗