Establishment of Precise Histological Evaluation Criteria for NASH Fibrosis Reversal

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorBeijing Municipal Administration of Hospitals

About this trial

Collect confirmed cases of NAFLD patients and enroll them in the study. Select patients with NASH and fibrosis stage F2-4 confirmed by liver biopsy, and collect clinical and pathological data for relevant evaluation and definition. Establish a NASH "fibrosis reversal" pathological evaluation system, based on a new reversal standard, establish non-invasive alternative indicators, and observe indicators.

Eligibility criteria

Qualifiers

Aged between 18 and 70 years at the time of liver biopsy;

Gender is not limited;

Hepatic perforation suggested that NASH complicated with fibrosis stage F2-4;

Signed written informed consent.

Disqualifiers

Combined HCV infection, HIV infection, alcoholic liver disease, autoimmune liver disease, genetic metabolic liver disease Disease, drug-induced liver injury and other chronic liver diseases;

Women during pregnancy;

There are the following conditions before liver perforation: HCC or possible HCC (imaging suggests malignant liver occupation); decompensation of cirrhosis (ascites, hepatic encephalopathy, gastrointestinal bleeding, hepatorenal syndrome, etc.); Patients with other malignant tumors; Recipients of liver transplantation;

Patients considered by the investigator to be unsuitable for this study.

Trial design

Treatments tested in this trial

  • life-style

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators

Beijing Municipal Administration of Hospitals

Lead sponsor

Beijing Ditan Hospital

Sponsor institution