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UnknownNCT05754242

Ascorbic Acid to Prevent Postreperfusion Syndrome in Liver Transplantation

Intravenous Vitamin C for the Prevention of Postreperfusion Syndrome in Orthotopic Liver Transplantation From Deceased Donors

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Hospital Universitario Ramon y Cajal · Academic / Other
Sex
All
Age
18 Years – 67 Years
Healthy volunteers
Not accepted

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.

Detailed 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

Conditions

Interventions

TypeNameDescription
DRUGAscorbic acid1.5 gr of ascorbic acid
DRUG0.9% Saline solution100 ml of 0.9% saline solution

Timeline

Start date
2020-11-17
Primary completion
2023-06-30
Completion
2023-07-30
First posted
2023-03-03
Last updated
2023-03-03

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT05754242. Inclusion in this directory is not an endorsement.

Ascorbic Acid to Prevent Postreperfusion Syndrome in Liver Transplantation (NCT05754242) · Clinical Trials Directory