Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT06567990 Sponsor: Hospices Civils de Lyon Condition: Non-Alcoholic Fatty Liver Disease
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Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT06567990
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:

  • People who have been diagnosed with type 2 diabetes
  • People aged between 40 and 80 years old
  • People who have been found to have fat build-up in the liver (hepatic steatosis), confirmed by a standard abdominal ultrasound scan, as defined by European liver disease guidelines
  • People who agree to take part and sign a consent form
  • People who are covered by a health insurance plan

Who may not be able to join:

  • People who have been diagnosed with cirrhosis (severe liver scarring), confirmed either by a liver biopsy showing the most advanced stage of scarring (F4), or by MRI scan
  • People who have another known cause of chronic liver disease, including: active Hepatitis B infection, previous or current Hepatitis C infection, autoimmune hepatitis, certain autoimmune bile duct disorders, Wilson disease, Alpha-1-antitrypsin deficiency, a condition causing iron build-up in the liver (haemochromatosis), liver damage caused by medications, or a blockage in the bile ducts
  • People who have taken medications known to cause liver fat build-up in the six months before the study
  • People with a known history of cirrhosis or signs of serious liver complications such as fluid build-up in the abdomen, confusion related to liver failure, or enlarged veins in the food pipe
  • People who have drunk alcohol regularly or heavily (more than 30g per day for men, or more than 15g per day for women) for more than two years at any point in the last ten years
  • People who are pregnant or currently breastfeeding
  • People whose life expectancy is less than 5 years
  • People with a known HIV infection
  • People who have type 1 diabetes
  • People with a BMI of 45 or above
  • People who are under legal guardianship or supervision due to mental health reasons
  • People who are currently detained or deprived of their liberty
  • People who do not understand French or are unable to give informed consent
  • People who are already taking part in another clinical trial that could interfere with this study, or who are within an exclusion period following a previous trial

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 28 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: 4 78 86 44 48

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
Registry
ClinicalTrials.gov
Start date
25 September 2024
Est. completion
25 May 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Progression of MASLD for T2D and MASLD patients without AF at baseline (cohort A) or progression to confirmed diagnosis of cirrhosis for T2D and MASLD patients with presence of AF at baseline and without cirrhosis (cohort B).

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: 28 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