Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT06626074 Sponsor: University Hospital, Angers Condition: Non-Alcoholic Fatty Liver Disease
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Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT06626074
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 are already part of the SNIFF patient group at Angers hospital, where fatty liver disease (NASH) is suspected and a liver biopsy and MRI scan have been requested by a liver specialist as part of their initial assessment
  • People who are adults (18 years of age or older)
  • People who have given their free and informed verbal agreement to take part in the study

Who may not be able to join:

  • People for whom an MRI scan is not safe or suitable (confirm with trial site)
  • People where more than 3 months have passed between the assessment of their liver condition and the MRI scan being done
  • People who are pregnant, in labour, or currently breastfeeding
  • People who are currently detained or restricted by a court or government authority
  • People who are receiving psychiatric care under compulsion (i.e., without their full free choice)
  • People who are under a legal protection order (confirm with trial site)
  • People who are not enrolled in or covered by a social security or health insurance scheme

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 27 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: Anita PAISANT, MD, University Hospital, Angers

Phone: 0241353637

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
University Hospital, Angers
Registry
ClinicalTrials.gov
Start date
5 September 2025
Est. completion
5 September 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Evaluation of the diagnostic performance of new MRI biomarkers for NASH diagnosis

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: 27 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