Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
NCT06843148

Stimulating Fat Tissue Storage With Niacin to Reduce Fat Accumulation in the Liver.

Led by Université de Sherbrooke · Updated on 2026-02-10

36

Participants Needed

1

Research Sites

221 weeks

Total Duration

On this page

Sponsors

U

Université de Sherbrooke

Lead Sponsor

C

CHU de Quebec-Universite Laval

Collaborating Sponsor

AI-Summary

What this Trial Is About

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 50 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

CONDITIONS

Official Title

Stimulating Fat Tissue Storage With Niacin to Reduce Fat Accumulation in the Liver.

Who Can Participate

Age: 50Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 50 to 80 years
  • Diagnosed with MASLD defined by liver steatosis and abdominal obesity according to International Diabetes Federation criteria
  • All women must be post-menopausal
Not Eligible

You will not qualify if you...

  • Advanced liver fibrosis (stage F3 or higher) or liver stiffness over 10 kPa
  • Serum ALT levels greater than three times the normal upper limit
  • Signs of portal hypertension
  • Other liver diseases besides MASLD
  • Previous diagnosis of diabetes
  • Overt cardiovascular or kidney disease, cancer (except non-melanoma skin cancer), or other uncontrolled medical conditions
  • Any contraindication to MRI
  • Previous intolerance or allergy to nicotinic acid
  • Participation in a research study involving radiation exposure within the past two years
  • Allergy to eggs
  • Smoking more than 1 cigarette per day or consuming more than 2 alcoholic beverages daily

AI-Screening

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Trial Site Locations

Total: 1 location

1

Centre de recherche du CHUS

Sherbrooke, Quebec, Canada, J1H 5N4

Actively Recruiting

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Research Team

F

Frédérique Frisch

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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