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Clinical Trial 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.


Clinical Trial Description

Researches will compared: - Incidence of postreperfusion syndrome in liver transplantation - Changes in interleukin values and other inflammatory markers before and after transplantation - Incidence of liver graft dysfunction between groups - Incidence of acute renal failure and other complications between groups ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05754242
Study type Interventional
Source Hospital Universitario Ramon y Cajal
Contact Luis Gajate, MD PhD
Phone +34913368269
Email gajate.luis@gmail.com
Status Recruiting
Phase Phase 2
Start date November 17, 2020
Completion date July 30, 2023

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