Non-Alcoholic Steatohepatitis (NASH)

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Review clinical trials related to Non-Alcoholic Steatohepatitis (NASH). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Empagliflozin Versus Statins in Non-Alcoholic Fatty Liver Disease

The goal of this clinical trial is to assess the efficacy of Empagliflozin versus Statins as monotherapy and polytherapy in non-alcoholic fatty liver disease and non-alcoholic Steatohepatitis. Does drug ABC Empagliflozin versus Statins as monotherapy and polytherapy improve the controlled attenuation parameter (CAP), the liver stiffness measurement (LSM), the proportion of patients with at least one point improvement or one-stage reduction in the histological scores with respect to hepatic steatosis, hepatocellular ballooning, lobular inflammation, and fibrosis after treatment? What medical problems do participants have when taking Empagliflozin versus Statins as monotherapy and polytherapy? Participants will: * Take Empagliflozin alone or Empagliflozin plus statins or Pioglitazone plus Statins or Pioglitazone alone as standard therapy every day for 3 months * Be directed to complete history taking. FibroScan®, abdominal ultrasound and laboratory tests of ALT, AST, ALP, platelets count, Triglycerides, Cholesterol, LDL, HDL, serum insulin and insulin resistance will be conducted at baseline and after the drug administration for 3 months. * Keep a diary of recording any side effects they use a rescue inhaler

Participants needed: 400
Trial details
Phase: Phase 4Age: 18-65Biological sex: AllType: InterventionalSponsor: Badr UniversityUpdated: Sep 18, 2025Locations: 1
Eligibility criteria

Adult [+4]

Pregnant women [+5]

Status: Recruiting

Longitudinal Observational Study Of Chinese With NAFLD/NASH

This is a 10-year, longitudinal, observational study of patients with NAFLD/NASH designed to specifically address important clinical questions that remain incompletely answered from registration trials. In addition to the study database, the biospecimen repository will also be included so that translational studies of genomics and biomarkers of response may be performed.

Participants needed: 20,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Humanity and Health Research CentreUpdated: Mar 24, 2025Locations: 1
Eligibility criteria

Males or females aged 18 and older; [+2]

Incompetent to understand and/or sign the informed consent; [+4]