drugset / Trial / NCT02930161

Runihol in Nonalcoholic Fatty Liver Disease and Metabolic Syndrome

NCT02930161 ↗

RandomizedParallel-groupTriple-blindTreatment

Summary

The study is designed to assess the safety and efficacy of different doses and dosing regimens of Runihol, tablets, enteric coated, produced by "NTFF" POLYSAN" (Russia), in prevention of liver disease progression in patients with non-alcoholic fatty liver disease and metabolic syndrome.

Timeline

Start
2016-05-30
Primary completion
2018-10-10
Completion
2018-10-10

Outcome

Outcome not reported

Stopped (Enrollment): “Low recruitment”

Drugs

EvaluationDrugModalityDoseRoute
Subject Runihol Unknown 1 unknown Oral
Subject Runihol Unknown 2 unknown Oral

Indications