Efficacy of Rifaximin on Hepatosteatosis and Steatohepatitis Patients
Fatty Liver, Steatohepatitis
About this trial
This is an interventional treatment trial for Fatty Liver focused on measuring Hepatosteatosis, Steatohepatitis, Rifaximin, Inflammatory cytokines
Eligibility Criteria
Inclusion Criteria:Patients between the ages of 18-70, irrespective of gender referred to the gastroenterology clinics for persistently elevated liver enzymes, obesity, T2DM (Type 2 diabetes mellitus) and clinical suspicion of NAFLD selected for this study
-
Exclusion Criteria:
Allergy for Rifaximin, pregnant women and lactating women, other liver diseases such as viral hepatitis, autoimmune liver diseases, drug induced liver diseases, pancreas-biliary tract and liver-related documented diseases (pancreatitis, stone pouch on the biliary colic pains, acute cholecystitis, choledocholithiasis, hepatobiliary cancers etc.,). Hit-defined psychiatric illness, excessive alcohol intake (who consume >20g/day ) were excluded from this study.
Sites / Locations
- Bezmialem Vakif University
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Hepatosteatosis
Steatohepatitis
Rifaximin was given to patients with hepatosteatosis in the doses of 3x2 daily, 200 mg tablets for 4 weeks.
Rifaximin was given to patients with steatohepatitis patients in the doses of 3x2 daily, 200 mg tablets for 4 weeks.