Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT04141592 Sponsor: Queen Mary University of London Condition: Non-Alcoholic Fatty Liver Disease
Back to Non Alcoholic Fatty Liver Disease

Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT04141592
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 aged 18 or older
  • People who have been diagnosed with non-alcoholic fatty liver disease (NAFLD) — a condition where excess fat builds up in the liver — confirmed by a doctor, a scan, or a liver tissue sample
  • People with NAFLD who also have Type 2 Diabetes may be included
  • People who have no liver condition of any kind, including no NAFLD, may be eligible to join as a healthy comparison participant — this would be confirmed using a specialist liver scan called a FibroScan (confirm with trial site)

Who may not be able to join:

  • People who are unwilling or unable to give their agreement to take part
  • People who have Type 1 Diabetes
  • People who have another form of liver disease besides NAFLD, such as viral hepatitis, autoimmune hepatitis, primary sclerosing cholangitis, primary biliary cholangitis, haemochromatosis, sarcoidosis, cystic fibrosis, or sickle cell disease
  • People who are taking medications known to affect liver function (except methotrexate)
  • People who have an autoimmune disease that, in the trial doctor's opinion, may interfere with immune system testing
  • People who are taking medications that suppress the immune system (except methotrexate, a short course of steroid tablets, or steroid inhalers)
  • People who are currently pregnant
  • People who have had a major organ transplant (corneal or hair transplants are not excluded)
  • People who regularly drink more than 14 units of alcohol per week (for women) or more than 21 units per week (for men)

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 26 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

Principal Investigator: William Alazawi, MD Phd, Queen Mary University of London

Phone: +442078822308

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
Queen Mary University of London
Registry
ClinicalTrials.gov
Start date
5 March 2019
Est. completion
31 July 2026

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Impact of weight loss surgery upon Non-alcoholic steatohepatitis

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: 26 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