Non-Alcoholic Fatty Liver Disease Trial, Recruiting NCT05974904 Sponsor: Chongqing Medical University Condition: Non-Alcoholic Fatty Liver Disease
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Non-Alcoholic Fatty Liver Disease Trial, Recruiting

NCT05974904
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 were part of the NHANES 2017–2020 survey (a large US national health study)
  • People who have been diagnosed with a liver condition called MAFLD (a type of fatty liver disease linked to metabolic health problems), based on one of the following:
  • People who have type 2 diabetes, identified by: taking medication to lower blood sugar, a blood sugar marker (HbA1c) of 6.5% or higher, a fasting blood sugar level of 7.0 mmol/L (126 mg/dL) or higher, or a blood sugar reading of 11.1 mmol/L (200 mg/dL) or higher two hours after a sugar drink
  • People who are overweight or obese, meaning a body mass index (BMI) of 25 or above for people of Caucasian background, or 23 or above for people of Asian background
  • People with a normal or lower BMI who have at least two of the following metabolic health concerns: a larger-than-normal waist measurement, high blood pressure or blood pressure medication use, high triglycerides (a type of fat in the blood) or medication for this, low "good" cholesterol (HDL) or medication for this, blood sugar levels in the prediabetes range, a high insulin resistance score (called HOMA-IR of 2.5 or above), or a raised inflammation marker in the blood (C-reactive protein above 2 mg/L)

Who may not be able to join:

  • People for whom liver ultrasound scan results are not available
  • People whose full health and clinical records are incomplete
  • People under 18 years of age
  • People who have been diagnosed with cancer

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: Tingqiu Wang, Bachelor, The Second Affiliated Hospital of Chongqing Medical University

Phone: +8617815370539

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Chongqing Medical University
Registry
ClinicalTrials.gov
Start date
18 July 2023
Est. completion
28 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Controlled attenuation parameter

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