RecruitingNot ApplicableNCT05874674

The Safety of Nafamostat Mesylate for Patients With High Risk Bleeding Undergoing Hemodialysis: A Pilot Study

The Safety of Nafamostat Mesylate for Patients With High Risk Bleeding Diathesis Undergoing Hemodialysis: A Pilot Study


Sponsor

Wonju Severance Christian Hospital

Enrollment

100 participants

Start Date

Dec 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Comparison nafamostat and low molecular weight heparin among dialysis patients


Eligibility

Min Age: 18 YearsMax Age: 99 Years

Inclusion Criteria1

  • platelet below 10k PTT above 60 second INR above 20 patient with bleeding (epistaxis, orbital bleeding, hematuria) recent brain hemorrhage (within 6 months) receiving anticoagulant therapy (coumadin or NOAC) dual antiplatelet agent users received major surgery within one month

Exclusion Criteria1

  • cancer liver cirrhosis pregnancy drug allergy current bleeding on major organ (brain, gastrointestinal)

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGNafamostat Mesylate

Comparison effect of nafamostat and cnoxan


Locations(1)

Yonsei Unviersity Wonju College of Medicin

Wŏnju, Kangwondo, South Korea

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05874674


Related Trials