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
| Type | Name | Description |
|---|---|---|
| DRUG | Tocotrienols / Vitamin E | Palm Tocotrienols complex |
| DRUG | Placebo control | Placebo 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.