Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT06035874 Sponsor: Medanta, The Medicity, India Condition: Non-Alcoholic Fatty Liver Disease
Back to Non Alcoholic Fatty Liver Disease

Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT06035874
Recruiting Not Applicable

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:

  • You are a man or woman aged 20 or older who has been diagnosed with type 2 diabetes for at least 3 months
  • You are currently taking standard diabetes medications (such as metformin, DPP-4 inhibitors, sulphonylureas, or insulin, alone or in combination) and your blood sugar control level (HbA1c) is below 9%
  • You have been confirmed to have fat in your liver (detected by a special type of MRI scan showing more than 5.6% fat)
  • You are in generally stable health based on your medical history, physical check-up, and blood tests
  • You are willing and able to follow all the rules and requirements of the study
  • You are willing to sign a consent form showing you understand and agree to take part

Who may not be able to join:

  • You have a history of type 1 diabetes, diabetic ketoacidosis (a serious diabetes emergency), a pancreas or insulin cell transplant, or diabetes caused by a pancreas problem or surgery
  • Your blood sugar levels are very unpredictable or difficult to control in a stable way
  • You have had a problem with drug or alcohol misuse in the past 3 years, score above 8 on an alcohol screening test, or have regularly drunk more than moderate amounts of alcohol (20g/day for women or 30g/day for men) for at least 3 months in the past 5 years
  • Your thyroid hormone level is too low or too high at the screening visit (confirm with trial site)
  • You have used certain diabetes or metabolic medications — including pioglitazone, SGLT2 inhibitors (e.g. canagliflozin, empagliflozin, dapagliflozin), GLP-1 medications (e.g. liraglutide, dulaglutide), or saroglitazar — within the past 12 weeks
  • Your BMI (body mass index) is over 40
  • You have an eating disorder, or your weight has changed by 5% or more (up or down) in the past 12 weeks
  • You have used weight loss medications or followed a formal weight loss programme recently (within the past 3–12 months)
  • You have kidney disease that needed immunosuppressive treatment, or you have had dialysis or a kidney transplant
  • You have had a heart attack, unstable chest pain, stroke, or certain heart or blood vessel procedures within the past 3 months, or you have been diagnosed with advanced heart failure (NYHA Class III or IV)
  • You have or have had hepatitis B, hepatitis C, or another active liver disease
  • You have used vitamin E supplements within the past 12 weeks
  • You have previously had bariatric (weight loss) surgery or major upper digestive tract surgery
  • You have a history of delayed stomach emptying (gastroparesis), poor nutrient absorption, inflammatory bowel disease, or another significant long-term gut condition
  • Your kidney filtering function (measured by a blood test called eGFR) is below 60 (confirm with trial site)
  • You have any metal objects in your body or any other reason you cannot safely have an MRI scan
  • You experience claustrophobia or anxiety about MRI scans, or you are unwilling to have MRI scans
  • You have a significant blood disorder (such as severe anaemia or low platelet count) at the time of screening
  • You have tested positive for HIV
  • You have had major surgery (requiring general anaesthesia) in the past 12 weeks, have not fully recovered from surgery, or are planning surgery during the study period
  • You have any medical reason that means you should not take the study drug, bempedoic acid (confirm with trial site)
  • You are currently taking or are likely to need steroid medications or immunosuppressive drugs

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 01244141414

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Medanta, The Medicity, India
Registry
ClinicalTrials.gov
Start date
15 October 2023
Est. completion
1 November 2024

Where this trial is recruiting

🇮🇳 India

Primary endpoints

The change in liver fat content

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov