drugset / Trial / NCT06127225

Proliverenol Supplementation for Non-Alcoholic Fatty Liver Disease (NAFLD)

NCT06127225 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a 4-arm, prospective, randomized, double-blind, double-dummy, and placebo-controlled clinical study comparing Proliverenol at a dose of 500 mg twice daily; Proliverenol at a dose of 1000 mg once daily; Proliverenol at a dose of 1000 mg twice daily; and Placebo two caplets daily for a 12-week course of therapy. Proliverenol is a bioactive fraction derived from the dried fruit of Phaleria macrocarpa (Scheff.) Boerl (Thymelaeaceae). Proliverenol possesses a hepatoprotective activity via anti-inflammation, DNA repairing, and the antiapoptosis properties.

Timeline

Start
2023-04-28
Primary completion
2024-08-09
Completion
2024-08-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Proliverenol Unknown 500 mg —
Subject Proliverenol Unknown 1000 mg —

Indications