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The Safety of Nafamostat Mesylate for Patients With High Risk Bleeding Undergoing Hemodial

Comparison nafamostat and low molecular weight heparin among dialysis patients

Condition(s)Dialysis; Complications, Bleeding
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryComparison nafamostat and low molecular weight heparin among dialysis patients
Who can participateInclusion Criteria: * 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 Criteria: * cancer liver cirrhosis pregnancy drug allergy current bleeding on major organ (brain, gastrointestinal)
Ages18 Years to 99 Years
SexAll
Accepts healthy volunteersYes
Lead sponsorWonju Severance Christian Hospital
LocationsWŏnju, Kangwondo, South Korea
Start date2023-12-01
NCT IDNCT05874674
Official listinghttps://clinicaltrials.gov/study/NCT05874674

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