About this trial
This study compares the effectiveness of the dietary supplement Gepaktiv with standard medications (UDCA and Ademetionine) in patients with fatty liver disease (MAFLD) and liver enlargement (hepatomegaly).
Key points:
* Participants will receive either Gepaktiv, UDCA, or Ademetionine for 15 days * Doctors will monitor liver health through blood tests and ultrasound scans * The study will check if Gepaktiv helps improve liver function as effectively as standard treatments.
Main measurements:
* Changes in liver enzyme levels (ALT, AST) * Reduction in liver size * Improvement in fat accumulation (steatosis) measured by FibroScan This research may provide evidence for a new natural option to support liver health.Data analysis will be done by an independent biostatistics
Eligibility criteria
Qualifiers
Age 18 to 65 years
Confirmed diagnosis of metabolic-associated fatty liver disease (MAFLD)
Hepatomegaly confirmed by ultrasound (≥3 cm craniocaudal liver enlargement)
ALT level between 90-150 U/L
Disqualifiers
Liver cirrhosis or hepatocellular carcinoma
Pregnancy or lactation
Known allergy to any of the study medications or supplement components
Gallstones or biliary obstruction
Trial design
Treatments tested in this trial
- Dietary supplement "Gepaktiv"
- UDCA (Ursodeoxycholic acid)
- Ademetionine