drugset / Trial / NCT03418935
Remaxol® in Mechanical Jaundice of Non-malignant Origin
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Remaxol | Unknown | 400 ml | Intravenous |
| Subject | Remaxol | Unknown | 800 ml | Intravenous |