# Efficacy of the nano curcumin supplementation on fibrosis, steatosis, inflammatory and metabolic status of liver fibrosis patients with non-alcoholic fatty liver origin: a study protocol for a double-blind randomized controlled trial

**Authors:** Hadis Gerami, Hassan Mozaffari-Khosravi, Asieh Mansour, Amir Ali Sohrabpour, Hossein Poustchi, Amir Pejman Hashemi Taheri, Mahmoud Reza Jaafari, Sara Jambarsang, Sayyed Saeid Khayyatzadeh

PMC · DOI: 10.1186/s40795-026-01252-0 · BMC Nutrition · 2026-02-02

## TL;DR

This study is testing if nano curcumin can improve liver health in patients with non-alcoholic fatty liver disease.

## Contribution

The study introduces a nano-formulated curcumin to overcome its poor bioavailability and tests its efficacy in liver fibrosis patients.

## Key findings

- The trial will assess fibrosis and steatosis using FibroScan before and after the intervention.
- Secondary outcomes include changes in inflammatory markers and metabolic parameters over 16 weeks.

## Abstract

Liver disease related to alcohol consumption and non-alcoholic fatty liver disease (NAFLD) are among the leading causes of liver fibrosis. Curcumin, due to its anti-fibrotic and anti-inflammatory effects, has been proposed as a potential therapeutic agent. However, its clinical application is limited by poor stability, solubility, and bioavailability. Nanocurcumin, a nano-formulated version of curcumin, overcomes these limitations. This study aims to evaluate the efficacy of Nanocurcumin supplementation in improving fibrosis, steatosis, inflammation, and metabolic status in patients with liver fibrosis of NAFLD origin.

This double-blind, randomized, placebo-controlled trial is being conducted at the Gastroenterology Clinic of Shariati Hospital (Tehran, Iran). Fifty patients aged 30 to 70 years are enrolled and randomly assigned to the intervention or placebo group using a block balanced randomization method. The intervention group receives one capsule of Nanocurcumin (40 mg, twice daily), while the placebo group receives an identical placebo capsule. The primary outcomes include liver fibrosis and steatosis, assessed via FibroScan at baseline and at the end of the study. Secondary outcomes include changes in inflammatory markers, metabolic parameters, liver function tests, anthropometric measures, and blood pressure over the 16-week intervention period.

This trial is currently ongoing. Recruitment is expected to be completed by the end of 2024, and the trial is anticipated to be fully completed by mid-2025. If Nanocurcumin supplementation demonstrates positive efficacy, it may serve as a potential therapeutic approach for patients with liver fibrosis.

Iranian Registry of Clinical Trials IRCT20210427051098N2 (Available from: https://irct.behdasht.gov.ir).

Date and version identifier: April 20, 2023; approved version by the IRCT.

The online version contains supplementary material available at 10.1186/s40795-026-01252-0.

## Linked entities

- **Chemicals:** curcumin (PubChem CID 969516)
- **Diseases:** non-alcoholic fatty liver disease (MONDO:0013209)

## Full-text entities

- **Diseases:** fibrosis (MESH:D005355), inflammatory (MESH:D007249), non-alcoholic fatty liver (MESH:D065626), steatosis (MESH:D005234), liver fibrosis (MESH:D008103)
- **Chemicals:** curcumin (MESH:D003474)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12955327/full.md

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Source: https://tomesphere.com/paper/PMC12955327