drugset / Trial / NCT05754242

Ascorbic Acid to Prevent Postreperfusion Syndrome in Liver Transplantation

NCT05754242 ↗

Phase 2 Unknown 70 enrolled Hospital Universitario Ramon y Cajal
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The goal of this clinical trial is to test the efficacy of intravenous ascorbic acid in preventing the postreperfusion syndrome in liver transplantation. The main questions it aims to answer are: * Can intravenous ascorbic acid prevent postreperfusion syndrome in liver transplantation ? * Can ascorbic acid decrease the incidence of liver graft dysfunction after liver transplantation? * Can ascorbic acid decreased the incidence of postoperative complications after liver transplantation ? Participants will receive 1.5 g of intravenous ascorbic acid diluted in 100 ml of saline or 100 ml of saline alone, during the anhepatic phase of liver transplantation before reperfusion of the new graft. Researchers will compared the incidence of postreperfusion syndrome in both groups.

Timeline

Start
2020-11-17
Primary completion
2023-06-30
Completion
2023-07-30

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

paper Data cleaning and analysis are expected to occur in the first months of 2024. PMID 38100226 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vitamin C Other / unclassified 1.5 g Intravenous

Indications

No indication recorded.