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Recruiting Not applicable

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

NCT05874674 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2023-12-01
Last updated
2024-07-30

Condition(s) studied

Dialysis; ComplicationsBleeding

Investigational drug(s) / intervention(s)

Nafamostat Mesylate →

Nafamostat Mesylate: Comparison effect of nafamostat and cnoxan

Study summary

Comparison nafamostat and low molecular weight heparin among dialysis patients

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
Accepted
Inclusion 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)

Primary outcome measure(s)

  • Number of patients with severe bleeding — 6 month
    Brain hemorrhage (on brain CT), gastrointestinal bleeding (on EGD)

Trial sites (1)

FacilityCityRegionStatus
Yonsei Unviersity Wonju College of Medicin Wŏnju Kangwondo Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05874674 on ClinicalTrials.gov ↗ ← All trials in South Korea