Effect of Sinbiotic With Multispecies Probiotics on Liver Parameters Liver Enzymes, Ultrasound, Elastography and Adipokines in Same Cases) in Patients With Metabolic Associated Steatotic Liver Disease.

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorEva Cubric

About this trial

Scientific hypothesis: the use of a synbiotic preparation with a multi-strain probiotic in patients with MASLD can lead to a decrease in non-invasive elastographic parameters of hepatic steatosis and fibrosis and an improvement in liver function.

The main objective of this study is to examine whether the test product affects the improvement of liver function measured by elastographic parameters or at least the prevention of further disease progression.

The goal of this clinical trial is to learn if sinbiotics works to improve liver function in adult patients with MASLD The main questions it aims to answer are:

Does sinbiotic lowers elastographic parameters od steatosis and fibrosis? Does it change liver function by lowering liver enzymes, blood lipids and sugar? Can sinbiotics lower CV risks and improve quality of life? Researchers will compare sinbiotic to a placebo (a look-alike substance that contains no drug) to see if sinbiotic works in MASLD patients.

Participants will:

Take sinbiotic or a placebo every day (td) for 9 months Visit the clinic once every 3 months for checkups, and at the begining and after 9 months for blood tests and US with elastography Keep a diary of their symptoms, diet, activity

Eligibility criteria

Qualifiers

MASLD confirmed by ultrasound and elastography with CAP > 260 dB/m/MHz;

other causes of chronic liver disease excluded and/or diagnosis confirmed by liver biopsy,

presence of metabolic syndrome according to the definition of the International Diabetes Federation (IDF): waist circumference for women over 80 cm or over 94 cm for men, and at least two of the other criteria (treated hypertensive or blood pressure > 130/85 mmHg determined during inclusion; treated diabetic or newly detected fasting serum glucose levels > 5.6 mmol/l; treated dyslipidemia or newly detected serum triglyceride levels > 1.7 mmol/L or HDL < 1.29 mmol/L for women/< 1.03 mmol/L for men),

signed informed consent.

Disqualifiers

pregnancy,

significant alcohol intake (>30g/day in men, >20g/day in women),

presence of autoimmune, viral, cholestatic (primary biliary cholangitis, primary sclerosing cholangitis, obstructive biliary tree diseases) or metabolic (hemochromatosis, Wilson) causes of chronic liver disease, transplant patients, malignant diseases, free fluid in the abdomen, significant small bowel resections,

signs of liver cirrhosis or LSM>13 kPa measured TE,

Trial design

Treatments tested in this trial

  • The test product is a ready-to-use sinbiotic preparation of multispecies probiotics, ca-butyrate and FOS
  • Placebo Drug

Treatment groups

114 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Eva Cubric

Lead sponsor

General Hospital Šibenik, Croatia

Sponsor institution

General Hospital Šibenik, Croatia

Collaborator

General Hospital Zadar

Collaborator

University Hospital Dubrava

Collaborator

University Hospital Rijeka

Collaborator

Clinical Hospital Merkur

Collaborator

University Hospital Sestre Milosrdnice

Collaborator

University Hospital of Split

Collaborator