Clinical Trials Directory

Trials / Completed

CompletedNCT01001403

Effect of Nafamostat on Postreperfusion Syndrome (PRS)

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

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
62 (actual)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

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

Conditions

Interventions

TypeNameDescription
DRUGNafamostat0.2 mg/kg as bolus 1 minute before reperfusion
DRUGNormal saline10 ml of normal saline

Timeline

Start date
2009-03-01
Primary completion
2010-03-01
Completion
2010-04-01
First posted
2009-10-26
Last updated
2010-05-11
Results posted
2010-05-03

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01001403. Inclusion in this directory is not an endorsement.