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Status unknownNCT00577044Updated Dec 17, 2008

Non Alcoholic Fatty Liver Disease (NAFLD) in Hong Kong

An observational study in Fatty Liver, sponsored by Hospital Authority, Hong Kong. Status unknown at 5 sites in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2008-12-17.

Sponsored by Hospital Authority, Hong Kong · Observational

The sponsor has not verified this record recently (last verified Jun 2008), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Enrollment
600
Ages
18 Years to 80 Years
Sex
All
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Study summary

The true incidence and prevalence of NAFLD in Hong Kong has not been determined. The natural history of NAFLD is not well defined partly because of differences in the exclusion limit of alcohol and the required histological criteria between studies. NAFLD is previously believed to be a benign non-progressive condition, but it has since been determined that a subset of patients can progress to cirrhosis and even hepatocellular carcinoma.

In fact in a recent histological review of NAFLD, fibrosis or liver cirrhosis was present in 15-50% of patients at index liver biopsy. The presence of obesity or type 2 diabetes mellitus are the strongest predictors of fibrosis. These same risk factors are also more common in patients with cryptogenic cirrhosis. Further evidence of the link between diabetes, obesity and NAFLD are mainly from the field of liver transplantation. In patients who underwent liver transplantation for cryptogenic liver cirrhosis, NAFLD recuured in a quarter of the hepatic allografts. The patients with recurrent NAFLD were more likely to be diabetic and had a higher body mass index (BMI) at the time of recurrent NAFLD. This suggests that NAFLD may have a significant role in the pathogenesis of crytogenic cirrhosis.

Although NAFLD was initially described as a slowly progressive disease, there are emerging data which shows that it can progress rapidly. Liver failure has even been described in patients with NAFLD after bariatric surgery, and a recent report described 5 cases of subacute liver failure in obese middle aged females with NAFLD related cirrhosis. NAFLD can also affect the progression of other diseases as well. Hepatic steatosis related to visceral obesity is a major independent risk factor for fibrogenesis related to chronic HCV hepatitis.

However, the prevalence of NAFLD and its interaction with chronic HBV, if any, is uncertain. This study aims to determine the prevalence of NAFLD in patients with unknown cause of hepatitis and to determine the histological fibrosis and inflammation in chronic HBV patients with NAFLD.

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Conditions studied

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In context

Liver Diseases

2,081 studies on the registry are indexed under Liver Diseases; 390 are open to participants now.

This study's planned enrollment of 600 is above the median of 167 across 681 observational studies indexed under Liver Diseases.

Browse Liver Diseases studies →

Lead sponsor

Hospital Authority, Hong Kong is the lead sponsor of 73 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All

Inclusion criteria

  • 18-80 years old
  • Gender: male and female

Exclusion criteria

Exclusion Criteria:

  • HBV patients and fatty liver HCV HIV
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Study design

Enrollment
600 participants (estimated)
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Study locations

5 sites
  • Department of Medicine, Queen Mary Hospital
    Hong Kong, China
  • Department of Pathology, Princess Margaret Hospital
    Hong Kong, China
  • Department of Pathology, Queen Elizabeth Hospital
    Hong Kong, China
  • Department of Pathology, Queen Mary Hospital
    Hong Kong, China
  • Department of Pathology, Tuen Mun Hospital
    Hong Kong, China
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 17, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00577044
Lead sponsor
Hospital Authority, Hong Kong
Collaborators
The University of Hong Kong
First posted
Dec 19, 2007
Start date
Jun 2004
Completion
Dec 2007 (estimated)
Last update
Dec 17, 2008

Study contacts

George K Lau, Dr
principal investigator · Department of Medicine, Queen Mary Hospital/ The University of Hong Kong
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2008. You cannot join it, but the record below documents what was studied.

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