Observational Study About Patients Diagnosed With NAFLD

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorXiangya Hospital of Central South University

About this trial

Nonalcoholic fatty liver disease (NAFLD) is the most common condition affecting the liver, owing to its association with obesity and the metabolic syndrome. The largest study to date using magnetic resonance spectroscopy to quantify liver triglyceride (TG) content showed that approximately 33% of individuals have hepatic steatosis. NAFLD encompasses a continuum of histological findings that starts with steatosis that can progress to nonalcoholic steatohepatitis (NASH), which is characterized by inflammation and cell death, and eventually cirrhosis. Given the large number of individuals afflicted with this condition, there is a clear need to develop effective and safe therapies to treat NAFLD.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

patients suspected of excessive alcohol consumption

malignant tumors, dementia, active tuberculosis, AIDS, organ failure, pregnancy or breastfeeding, etc cannot cooperate with the investigation

incomplete data such as HBV serological results and abdominal ultrasound results

patients who refuse to sign informed consent

Trial population

Patients between the age of 18-75, who was diagnosed with NAFLD were all elligible for this observational study.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

500 Participants
are grouped into 1 trial group
Group A: Patients diagnosed with NAFLD

Trial outcomes

Primary outcomes

1

BMI

BMI stands for body mass index. This is the ratio of a person's height to their weight.

Time frame
3 weeks
2

alcohol intake

alcohol consumption every week

Time frame
3 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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