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Assessment of lipid profile in patients with fatty liver disease.

Not Applicable
Completed
Conditions
Health Condition 1: K760- Fatty (change of) liver, not elsewhere classified
Registration Number
CTRI/2023/06/054482
Lead Sponsor
Tushar Akare
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
105
Inclusion Criteria

Evidence of fatty liver on ultrasonography of abdomen.

Patients who satisfy the European Association for the Study of the Liver Criteria (EASL criteria) for NAFLD will be recruited for the study.

EASL criteria for NAFLD is alcohol consumption less than 30 g/day for men and less than 20 g/day for women.

Age >18 years and <65 years of any gender.

Exclusion Criteria

Subjects having significant alcohol consumption (more than 30 gm/day in case of males and more than 20 gm/day in case of females)

Pregnant or lactating women

Subjects carrying hepatitis B and/or hepatitis C virus infection

Patients with autoimmune hepatic disease

Other chronic hepatic diseases i.e. Wilson’s disease, hereditary hemochromatosis, primary billiary cirrhosis etc.

Patients on drugs that can lead to fatty liver e.g. methotrexate, amiodarone, anti- retroviral drugs, tamoxifene, barium salts, tetracycline, Estrogen, glucocorticoids, etc.

Individuals having DM, metabolic syndrome, dyslipidemia and/or hypothyroidism

Individuals having significant alcohol consumption and/or CLD

Pregnant or lactating women.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fasting triglyceride <br/ ><br>Fasting glucose <br/ ><br>Triglyceride glucose index <br/ ><br>Liver ElastographyTimepoint: Baseline
Secondary Outcome Measures
NameTimeMethod
Severity of diseaseTimepoint: Baseline
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