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NCT06913699Active, not recruiting

The Ameliorative Effect of C-Kit (+) Hepatic Endothelial Cells With Mertk Deficiency on Nonalcoholic Steatohepatitis

Source: ClinicalTrials.gov · Last updated 8 Apr 2025

Brief summary (registry, in English)

The prevalence of non-alcoholic fatty liver disease (NAFLD) has been steadily increasing, with 10-20% of affected individuals progressing to non-alcoholic steatohepatitis (NASH). NASH is pathologically characterized by hepatic inflammation, steatosis, and hepatocyte injury. Furthermore, this condition carries a significant risk of progression to advanced hepatic fibrosis (pathological Scheuer fibrosis stage F≥3), cirrhosis, and even hepatocellular carcinoma (HCC). In recent years, NASH has emerged as the leading contributor to the growing burden of cirrhosis worldwide, representing a major public health challenge. Despite the high incidence and clinical severity of NAFLD, there are currently no FDA-approved therapeutic agents for its management. Therefore, elucidating the molecular mechanisms underlying NAFLD-associated NASH progression is critical for developing targeted pharmacological interventions capable of preventing, ameliorating, or potentially reversing disease progression.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
6 (estimated)
First submitted
30 Mar 2025
Start date
1 Apr 2024
Primary completion date
30 Apr 2026
Lead sponsor
Shanghai East Hospital
NCT number
NCT06913699

What you commit to

  • Study type: Observational
  • Planned participants: 6
  • From 1 Apr 2024 to the primary completion date, 30 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Active viral hepatitis (HBV, HCV)
  • Recent history of illicit drug use

Other

  • Cirrhosis (compensated or decompensated)
  • Hepatocellular carcinoma
  • Primary biliary cholangitis
  • Primary sclerosing cholangitis
  • Alcohol intake≥20 g/day for women and ≥30 g/day for men
  • Current pregnancy or breastfeeding
  • Severe comorbidities.

Who the study is looking for

  • Clinical diagnosis of Non-Alcoholic Fatty Liver Disease
  • Age 18-65 years

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shanghai East Hospital (East Hospital Affiliated to Tongji University)
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.