Non-Alcoholic Fatty Liver Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People between 25 and 55 years old
- People who are willing to sign a consent form agreeing to take part as a research participant
- People who are able and willing to take supplements by mouth at set times throughout the study
- People who are willing to keep a diary to record whether they have taken their supplements as instructed
- People who have been diagnosed with a liver condition called MAFLD (metabolic-associated fatty liver disease), confirmed by a specialist using a scan called FibroScan, with a specific fat measurement result (CAP score) of 263 dB/m or higher
Who may not be able to join:
- People who have hepatitis B, hepatitis C, autoimmune hepatitis, alcoholic liver disease, or liver cirrhosis
- People who are pregnant, breastfeeding, or planning to become pregnant during the study
- People with a history of drinking more than 40 grams of alcohol per day
- People who have had serious liver-related complications, including fluid build-up in the abdomen (ascites), brain function problems linked to liver disease (encephalopathy), or bleeding from swollen veins in the digestive tract
- People who have been diagnosed with liver cancer (hepatocellular carcinoma)
- People who have had bowel removal surgery or weight-loss surgery, or who have a chronic inflammatory bowel condition such as Crohn's disease or ulcerative colitis
- People who have taken antibiotics, probiotics, prebiotics, or synbiotics within the past month
- People who are currently using Vitamin E or omega-3 fatty acid supplements
- People who were not hospitalised in the past month and therefore had no dietary restrictions related to illness (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Hery D Purnomo, Dr, Dr. Kariadi Medical Hospital
Phone: +628122803136
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Complete Hematology; Metabolic Profile; Metabolic Profile; Metabolic Profile; Insulin; TNF-alpha; CRP (C-Reactive Protein)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.