Clinical Trials Directory

Trials / Completed

CompletedNCT04704063

Efficacy and Safety of Tocovid Suprabio 200mg in Non-alcoholic Fatty Liver (NAFL)

A Randomized, Double-Blind, Placebo-Controlled Study, to Assess the Efficacy and Safety of Tocovid Suprabio 200mg in Non-alcoholic Fatty Liver (NAFL)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
170 (actual)
Sponsor
Yuen Kah Hay · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Palm-derived tocotrienols have shown hepatoprotective effects in both animal and human studies. This study aims to investigate the effects of tocotrienols in hepatocellular lipid content using MRI. Non-alcoholic fatty liver disease (NAFLD) is a spectrum of diseases ranging from simple fatty liver (steatosis, NAFL) to non-alcoholic steatohepatitis (NASH) to cirrhosis. NASH is the accumulation of fat in liver cells accompanied with inflammation that can lead to the scarring of the liver. Prevention of liver fibrosis by early introduction of low risk interventions such as lifestyle modification, diet control and nutraceuticals may help circumvent long-term healthcare costs associated with management of chronic NASH.

Conditions

Interventions

TypeNameDescription
DRUGTocotrienols / Vitamin EPalm Tocotrienols complex
DRUGPlacebo controlPlacebo matching Tocovid Suprabio

Timeline

Start date
2021-01-01
Primary completion
2023-08-15
Completion
2023-10-01
First posted
2021-01-11
Last updated
2024-05-10

Locations

4 sites across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT04704063. Inclusion in this directory is not an endorsement.