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Thyroid Dysfunction and Its Association With Metabolic Dysfunction-Associated Fatty Liver Disease

Thyroid Dysfunction and Its Association With Metabolic Dysfunction-Associated Fatty Liver Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06739330
Enrollment
150
Registered
2024-12-18
Start date
2024-12-19
Completion date
2025-05-01
Last updated
2024-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Dysfunction-Associated Fatty Liver Disease, Thyroid Dysfunction

Brief summary

This study aims to evaluate the prevalence of thyroid dysfunction and its association with metabolic dysfunction-associated fatty liver disease.

Detailed description

One of the most common causes of chronic liver diseases worldwide is metabolic dysfunction-associated fatty liver disease (MAFLD), which affects about 30% of adults. Thyroid hormones are critical in maintaining metabolic homeostasis throughout life and are intimately linked to the liver. Dysfunctions of the thyroid gland have been implicated as one of the most important risk factors of MAFLD due to its important role in the hepatic synthesis of fatty acid and cholesterol. Maintaining liver metabolism requires thyroid function to be normal, while thyroid disorders may lead to liver disease progression.

Interventions

DEVICEFibroscan

Fibroscan will be used to assess the stages of fibrosis and steatosis using Dimensional ultrasound TE (transient elastography). Dimensional ultrasound TE (transient elastography) will be used for staging liver fibrosis and steatosis by measuring the velocity of a low frequency (50 Hz) elastic shear wave propagating through the liver.

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 18 years. * Both sexes. * Patients with metabolic dysfunction-associated fatty liver disease (MAFLD).

Exclusion criteria

* History of thyroid disease or treatment (e.g., thyroid nodules, thyroid cancer, hypothyroidism, and hyperthyroidism). * Patients with alcoholic liver disease take more than 40g of alcohol (or four units) per day. * Viral hepatitis. * Pregnant women.

Design outcomes

Primary

MeasureTime frameDescription
Level of free triiodothyronine (FT3)After the sample is taken (up to 5 minutes)Free triiodothyronine (FT3) will be measured using chemiluminescent immunoassay analysis.

Secondary

MeasureTime frameDescription
Level of free thyroxine (FT4)After the sample is taken (up to 5 minutes)Free thyroxine (FT4) will be measured using chemiluminescent immunoassay analysis.
Level of thyroid stimulating hormoneAfter the sample is taken (up to 5 minutes)Thyroid stimulating hormone will be measured using chemiluminescent immunoassay analysis.
Relation between gender and thyroid functionAfter the sample is taken (up to 5 minutes)Relation between gender and thyroid function will be assessed.
Correlation between metabolic data and thyroid function testsAfter the sample is taken (up to 5 minutes)Correlation between metabolic data and thyroid function tests will be assessed.

Countries

Egypt

Contacts

Primary ContactShimaa A Meshaal, MD
shaimaa.meshaal2013@med.tanta.edu.eg00966559806580

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026