Under construction – not a live service
Sign in
Taking people in ChinaNo phase

Studying liver tissue and blood to understand how the liver deteriorates in liver disease

Examines blood and leftover liver tissue from people with fatty liver, fibrosis or HBV.

Plain-language title generated from the registry record
Registry title: Single-cell Multiomics and Spatiotemporal Omics Analyze the Mechanism of Liver Degenerative Disease

Key facts

Where
Guangzhou, ChinaSee the site

Where in China

  • NanGuangzhou, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Nanfang Hospital, Southern Medical University
Trial code
NCT07265544
Record updated
14 April 2026
Original description
The purpose of this observational study is to employ single-cell multi-omics and spatial omics technologies to characterize the spatial and immune structures within the livers of patients with fatty liver, hepatic hemangioma, focal nodular hyperplasia, liver fibrosis, cirrhosis, and HBV infection. The primary questions it aims to address are:Read full original descriptionShow less

Single-cell Multiomics and Spatiotemporal Omics Analyze the Mechanism of Liver Degenerative Disease

The purpose of this observational study is to employ single-cell multi-omics and spatial omics technologies to characterize the spatial and immune structures within the livers of patients with fatty liver, hepatic hemangioma, focal nodular hyperplasia, liver fibrosis, cirrhosis, and HBV infection. The primary questions it aims to address are:

Investigate the mechanisms of liver degenerative changes during the processes of liver aging, fatty liver, HBV infection, liver fibrosis, and cirrhosis.

Characterize the molecular features and cellular networks at different stages of liver degeneration and identify new targets and mechanisms for the cure of the aforementioned diseases.

The study will collect peripheral blood and discarded liver tissue from patients with hepatic hemangioma, fatty liver, HBV infection, liver fibrosis, and cirrhosis who are undergoing hepatectomy or liver biopsy.

Inclusion: Voluntarily signed the informed consent form; No restrictions on age and gender; Patients diagnosed with hepatic hemangioma or focal nodular hyperplasia of the liver in accordance with the "Guidelines for the Diagnosis and Treatment of Focal Liver Lesions (2014 Edition)" and the "Guidelines for the Diagnosis and Treatment of Hemangiomas and Vascular Malformations (2019 Edition)"; Patients with hepatic hemangioma, focal nodular hyperplasia of the liver, fatty liver, HBV infection, liver fibrosis, and cirrhosis who clinically require liver surgery or liver biopsy.

Exclusion: Individuals with concurrent infections such as HIV will be excluded; Patients with coagulation system disorders, such as hemophilia or idiopathic thrombocytopenic purpura, will not be included; Those with severe underlying diseases that affect the body's immune status will be excluded; Individuals whom the investigator deems unsuitable for participation in this study will be excluded.

ClinicalTrials.gov NCT07265544