About this trial
Metabolic dysfunction-associated steatotic liver disease (MASLD) (aka non-alcoholic fatty liver disease), commonly occurring in individuals with obesity and type 2 diabetes can lead to liver inflammation/ fibrosis. MASLD results from fat being disproportionately deposited in the liver.
The goal of this mechanistic study is to investigate metabolic response in patients aged 20 to 80 years with non-alcoholic fatty liver disease, after niacin (vitamin B3) treatment.
The main questions it aims to answer are:
* Does Niacin lower the fat deposition in the liver? * Does Niacin raise White Adipose Tissue storage of dietary fatty acids?
Researchers will compare Niacin to a placebo (a look-alike substance that contains no drug) to compare the metabolic response.
Duration of study per participant: Up to 28 weeks
Eligibility criteria
Qualifiers
aged 20 to 80 years;
diagnosed with MASLD, defined as the presence of liver steatosis + abdominal obesity (as defined by the International Diabetes Federation country/ethnic group-specific criteria;
Disqualifiers
None
Trial design
Treatments tested in this trial
- Niacin (250mg)
- Placebo Oral Tablet
Treatment groups
Sponsors and collaborators
Université de Sherbrooke
Lead sponsor
CHU de Quebec-Universite Laval
Collaborator
Centre de recherche du Centre hospitalier universitaire de Sherbrooke
Collaborator