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
| Type | Name | Description |
|---|---|---|
| DRUG | Nafamostat | 0.2 mg/kg as bolus 1 minute before reperfusion |
| DRUG | Normal saline | 10 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.