drugset / Trial / NCT03418935

Remaxol® in Mechanical Jaundice of Non-malignant Origin

NCT03418935 ↗

RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the safety and efficacy of Remaxol (succinate + methionine + inosine + nicotinamide; POLYSAN Ltd., Russia) infusions at dose 400 and 800 ml to treat mechanical jaundice of non-tumor cause during the first week after surgery.

Timeline

Start
2017-04-03
Primary completion
2020-03-31
Completion
2020-04-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Remaxol Unknown 400 ml Intravenous
Subject Remaxol Unknown 800 ml Intravenous

Indications