Clinical trial Recruiting at 1 site Observational Ages 18 and up

NAFLD in Obese Chinese Patients Undergoing Bariatric Surgery

Official title: Clinical Course and Biomarkers Associated With Nonalcoholic Fatty Liver Disease (NAFLD) in Chinese Patients With Obesity

Run by Chinese University of Hong Kong · NCT07662356 · Data updated 2026-11-12

This study tests how NAFLD progresses and which biomarkers appear in obese Chinese adults undergoing laparoscopic bariatric surgery.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment200 (estimated)
SponsorChinese University of Hong Kong
Academic / other
Locations1 site (Hong Kong, New Territories)
StatusRecruiting
StartedDecember 16, 2019
Main results expectedOctober 19, 2028
Study endsDecember 31, 2030
Registry record updatedJune 23, 2026
Trial IDNCT07662356 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older, of Chinese ethnicity, undergoing obesity surgery at Prince of Wales Hospital, with or without known NAFLD at baseline.

Probably not a fit

Patients with alcohol-related liver disease, other liver conditions, or those unwilling to consent may not benefit from the study findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study follows Chinese adults with obesity who are undergoing laparoscopic bariatric surgery to explore the clinical course of NAFLD and related biomarkers. Liver biopsies are taken during surgery for histology and scoring, with comprehensive clinical and biochemical assessments before and after the procedure. The aim is to better understand how NAFLD progresses toward more advanced liver disease in this population and identify factors linked to its development. Participants are followed within the surgical care pathway at Prince of Wales Hospital, CUHK, under an institutional lead by CUHK. The study does not assign an intervention beyond standard surgical care, and data collected will help clarify disease progression and potential biomarker signatures.

Why it matters

Potential benefit: Findings could improve understanding of NAFLD progression and identify biomarkers that help predict who is at higher risk for liver disease progression.

How similar studies have gone: Prior research in bariatric populations has shown liver biopsy can reveal NAFLD/NASH features; this study adds longitudinal biomarker assessment in a Chinese cohort.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 years or above
* Chinese ethnicity
* Patient undergoing obesity surgery at The Prince of Wales Hospital

Exclusion Criteria:

* Endocrine causes of obesity
* Active uncontrolled psychiatric illness
* Active substance abuse
* Alcohol intake exceeding 30 grams per day in males or 20 grams per day in females
* Presence of other co-existing liver disease, as evidenced by known history of positive viral hepatitis serology
* History of decompensated liver disease
* Unlikely to comply with management protocol
* Failure to give consent

Where it's running

  • Department of Medicine and Therapeutics, The Chinese University of Hong Kong (CUHK), Ward 3M, Diabetes and Endocrine Research Centre, 3/F Day Treatment Block and Children Wards (Old Block), Prince of Wales Hospital
    Hong Kong, New Territories, Hong Kong
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.