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Effect of Nafamostat on Postreperfusion Syndrome (PRS)

Liver Transplantation Clinical Trial

Official title:
Effect of Nafamostat Mesilate on Hemodynamic Stability After Reperfusion of the Liver Graft

Clinical Trial Summary

This study intends to see the effect of nafamostat on the attenuation of postreperfusion syndrome (PRS) that frequently occurs during liver transplantation.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01001403
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase Phase 4
Start date March 2009
Completion date April 2010
View Details
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